publisci 0.1.3 → 0.1.4
This diff represents the content of publicly available package versions that have been released to one of the supported registries. The information contained in this diff is provided for informational purposes only and reflects changes between package versions as they appear in their respective public registries.
- checksums.yaml +4 -4
- data/Gemfile +2 -2
- data/LICENSE.txt +19 -17
- data/README.md +41 -8
- data/README.rdoc +3 -5
- data/Rakefile +2 -2
- data/bin/publisci +9 -7
- data/examples/visualization/prov_viz.rb +1 -1
- data/lib/publisci.rb +19 -11
- data/lib/publisci/datacube_model.rb +2 -2
- data/lib/publisci/dataset/ORM/data_cube_orm.rb +2 -2
- data/lib/publisci/dataset/data_cube.rb +1 -1
- data/lib/publisci/dataset/dataset_for.rb +6 -1
- data/lib/publisci/dataset/interactive.rb +1 -46
- data/lib/publisci/generators/base.rb +22 -0
- data/lib/publisci/generators/maf.rb +172 -0
- data/lib/publisci/metadata/generator.rb +1 -1
- data/lib/publisci/parser.rb +62 -62
- data/lib/publisci/parsers/base.rb +29 -0
- data/lib/publisci/parsers/maf.rb +20 -0
- data/lib/publisci/readers/arff.rb +43 -43
- data/lib/publisci/readers/base.rb +2 -2
- data/lib/publisci/readers/csv.rb +2 -1
- data/lib/publisci/readers/maf.rb +15 -181
- data/lib/publisci/readers/r_matrix.rb +143 -143
- data/lib/publisci/writers/arff.rb +1 -1
- data/lib/publisci/writers/base.rb +1 -1
- data/resources/maf_rdf.ttl +98 -22
- data/spec/ORM/data_cube_orm_spec.rb +1 -1
- data/spec/ORM/prov_model_spec.rb +3 -3
- data/spec/dataset_for_spec.rb +1 -1
- data/spec/generators/maf_spec.rb +2 -1
- data/spec/maf_query_spec.rb +1 -1
- metadata +25 -23
- data/lib/r2rdf.rb +0 -226
- data/lib/template_bak.rb +0 -12
@@ -1,54 +1,54 @@
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module PubliSci
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module Readers
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class RMatrix
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include PubliSci::Dataset::DataCube
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#NOTE; this is pretty much hard coded for Karl's application right now, and doesn't
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# do any dimension or code generation. Since its a set of LOD scores indexed by dimension
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# and marker the usual datacube generator wont work (I think). In the future adding an option
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# to specify this kind of a dataset would probably be useful
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def generate_n3(client, var, outfile_base, options={})
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meas = measures(client,var,options)
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dim = dimensions(client,var,options)
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codes = codes(client,var,options)
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outvar = sanitize([var]).first
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probes_per_file = options[:probes_per_file] || 100
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col_select = "colnames"
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col_select = "names" if options[:type] == :dataframe
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#write structure
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open(outfile_base+'_structure.ttl','w'){|f| f.write structure(client,var,outvar,options)}
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probes=client.eval("#{col_select}(#{var})").to_ruby
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if probes == nil
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client.eval("colnames(#{var})=1:ncol(#{var})")
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probes=client.eval("#{col_select}(#{var})").to_ruby
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end
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markers = rows(client,var,options)
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if options[:print]
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puts prefixes(var,options)
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end
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if options[:output] == :string
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str = prefixes(var,options)
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end
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probes.each_with_index{|probe,i|
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#write prefixes and erase old file on first run
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unless options[:print] || options[:output] == :string
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open(outfile_base+"_#{i/probes_per_file}.ttl",'w'){|f| f.write prefixes(var,options)} if i % probes_per_file == 0
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end
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i+=1
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obs_data = observation_data(client,var,i,markers,options)
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labels = labels_for(client,var,probe)
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# labels = sanitize(labels)
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# return obs_data
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if options[:print]
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observations(meas,dim,codes,obs_data,labels,outvar,options).each{|obs| puts obs}
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end
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end
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unless options[:print] || options[:output] == :string
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open(outfile_base+"_#{i/probes_per_file}.ttl",'a'){|f| observations(meas,dim,codes,obs_data,labels,outvar,options).map{|obs| f.write obs}}
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puts "#{i}/#{probes.size}" unless options[:quiet]
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end
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}
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if options[:output] == :string
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str
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end
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end
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def structure(client,var,outvar,options={})
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meas = measures(client,var,options)
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dim = dimensions(client,var,options)
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codes = codes(client,var,options)
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str = prefixes(var, options)
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str << data_structure_definition(meas,[],codes,outvar,options)
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str << dataset(outvar,options)
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component_specifications(meas, dim, codes, var, options).map{ |c| str << c }
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measure_properties(meas,var,options).map{|m| str << m}
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str
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end
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#for now just make everything a measure
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def measures(client, var, options={})
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if options[:measures]
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options[:measures]
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else
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["probe","marker","value"]
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end
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# measure_properties(measures,var,options)
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end
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def dimensions(client, var, options={})
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# dimension_properties([""],var)
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[]
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end
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def codes(client, var, options={})
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[]
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end
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def labels_for(connection,var,probe_id,options={})
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row_names = connection.eval("row.names(#{var})")
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# row_names = (1..@rexp.payload.first.to_ruby.size).to_a unless row_names.first
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if row_names == connection.eval('NULL')
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row_names = (1..connection.eval("nrow(#{var})").payload.first).to_a
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else
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row_names = row_names.payload
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end
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labels = (1..(row_names.size)).to_a.map(&:to_s)
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labels = labels.map{|l|
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l.insert(0,probe_id.to_s + "_")
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}
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labels
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end
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def rows(connection,var,options={})
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row_names = connection.eval("row.names(#{var})")
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#hacky solution because rserve client's .to_ruby method doesn't fully work
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if row_names == connection.eval('NULL')
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row_names = (1..connection.eval("nrow(#{var})").payload.first).to_a
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else
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row_names = row_names.payload
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end
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row_names
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end
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def observation_data(client, var, probe_number, row_names, options={})
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data = {}
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# geno_chr = client.eval("#{var}$geno$'#{chr}'")
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# n_individuals = client.eval("#{var}$pheno[[1]]").to_ruby.size
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# entries_per_individual = @rexp.payload["geno"].payload[row_individ].payload["map"].payload.size * @rexp.payload["geno"].payload.names.size
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col_label = "probe"
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row_label = "marker"
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val_label = "value"
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if options[:measures]
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col_label = options[:measures][0] || "probe"
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row_label = options[:measures][1] || "marker"
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val_label = options[:measures][2] || "value"
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end
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data["#{col_label}"] = []
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data["#{row_label}"] = []
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data["#{val_label}"] = []
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# n_individuals.times{|row_individ|
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# puts "#{row_individ}/#{n_individuals}"
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col_select = "colnames"
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col_select = "names" if options[:type] == :dataframe
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if options[:type] == :dataframe
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probe_obj = client.eval("#{var}[[#{probe_number}]]").to_ruby
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else
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probe_obj = client.eval("#{var}[,#{probe_number}]").to_ruby
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end
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# puts probe_obj
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probe_id = client.eval("#{col_select}(#{var})[[#{probe_number}]]").to_ruby
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data["#{col_label}"] = (1..(probe_obj.size)).to_a.fill(probe_id)
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probe_obj.each_with_index{|lod,i|
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data["#{row_label}"] << row_names[i]
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data["#{val_label}"] << lod
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}
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data.map{|k,v| v.flatten!}
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data
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end
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end
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end
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end
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data/resources/maf_rdf.ttl
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@base <http://onto.strinz.me/dc/dataset/
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@prefix ns: <http://onto.strinz.me/dc/dataset/
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@base <http://onto.strinz.me/dc/dataset/MAF_ah1iit/> .
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@prefix ns: <http://onto.strinz.me/dc/dataset/MAF_ah1iit/> .
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@prefix qb: <http://purl.org/linked-data/cube#> .
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@prefix rdf: <http://www.w3.org/1999/02/22-rdf-syntax-ns#> .
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@prefix rdfs: <http://www.w3.org/2000/01/rdf-schema#> .
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@prefix prop: <http://onto.strinz.me/properties/> .
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@prefix dct: <http://purl.org/dc/terms/> .
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@prefix xsd: <http://www.w3.org/2001/XMLSchema#> .
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@prefix cs: <http://onto.strinz.me/dc/dataset/
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@prefix code: <http://onto.strinz.me/dc/dataset/
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@prefix cs: <http://onto.strinz.me/dc/dataset/MAF_ah1iit/cs/> .
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@prefix code: <http://onto.strinz.me/dc/dataset/MAF_ah1iit/code/> .
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@prefix owl: <http://www.w3.org/2002/07/owl#> .
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@prefix skos: <http://www.w3.org/2004/02/skos/core#> .
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@prefix foaf: <http://xmlns.com/foaf/0.1/> .
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@prefix org: <http://www.w3.org/ns/org#> .
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@prefix prov: <http://www.w3.org/ns/prov#> .
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ns:dsd-
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ns:dsd-MAF_ah1iit a qb:DataStructureDefinition;
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qb:component cs:Variant_Classification ;
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qb:component cs:Variant_Type ;
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qb:component cs:dbSNP_Val_Status ;
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qb:component cs:patient_id ;
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qb:component cs:sample_id .
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ns:dataset-
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rdfs:label "
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qb:structure ns:dsd-
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ns:dataset-MAF_ah1iit a qb:DataSet ;
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rdfs:label "MAF_ah1iit"@en ;
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qb:structure ns:dsd-MAF_ah1iit .
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cs:Variant_Classification a qb:ComponentSpecification ;
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rdfs:label "Variant_Classification" ;
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rdfs:label "Entrez_Gene_Id"@en .
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prop:Center a rdf:Property, qb:MeasureProperty ;
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rdfs:label "Center"@en
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rdfs:range xsd:string .
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rdfs:label "Center"@en .
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prop:NCBI_Build a rdf:Property, qb:MeasureProperty ;
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rdfs:label "NCBI_Build"@en
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rdfs:range xsd:int .
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rdfs:label "NCBI_Build"@en .
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prop:Chromosome a rdf:Property, qb:MeasureProperty ;
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rdfs:label "Chromosome"@en
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rdfs:range xsd:int .
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rdfs:label "Chromosome"@en .
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prop:Start_Position a rdf:Property, qb:MeasureProperty ;
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rdfs:label "Start_Position"@en .
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rdfs:label "dbSNP_RS"@en .
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prop:Tumor_Sample_Barcode a rdf:Property, qb:MeasureProperty ;
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rdfs:label "Tumor_Sample_Barcode"@en
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-
rdfs:range xsd:string .
|
240
|
+
rdfs:label "Tumor_Sample_Barcode"@en .
|
245
241
|
|
246
242
|
prop:Matched_Norm_Sample_Barcode a rdf:Property, qb:MeasureProperty ;
|
247
243
|
rdfs:label "Matched_Norm_Sample_Barcode"@en .
|
@@ -955,7 +951,7 @@ code:sequencer a skos:ConceptScheme;
|
|
955
951
|
skos:inScheme code:sequencer .
|
956
952
|
|
957
953
|
ns:obs2 a qb:Observation ;
|
958
|
-
qb:dataSet ns:dataset-
|
954
|
+
qb:dataSet ns:dataset-MAF_ah1iit ;
|
959
955
|
prop:Variant_Classification <code/variant_classification/Missense_Mutation> ;
|
960
956
|
prop:Variant_Type <code/variant_type/SNP> ;
|
961
957
|
prop:dbSNP_Val_Status <code/dbsnp_val_status/> ;
|
@@ -990,7 +986,7 @@ ns:obs2 a qb:Observation ;
|
|
990
986
|
.
|
991
987
|
|
992
988
|
ns:obs3 a qb:Observation ;
|
993
|
-
qb:dataSet ns:dataset-
|
989
|
+
qb:dataSet ns:dataset-MAF_ah1iit ;
|
994
990
|
prop:Variant_Classification <code/variant_classification/Missense_Mutation> ;
|
995
991
|
prop:Variant_Type <code/variant_type/SNP> ;
|
996
992
|
prop:dbSNP_Val_Status <code/dbsnp_val_status/byFrequency> ;
|
@@ -1025,7 +1021,7 @@ ns:obs3 a qb:Observation ;
|
|
1025
1021
|
.
|
1026
1022
|
|
1027
1023
|
ns:obs4 a qb:Observation ;
|
1028
|
-
qb:dataSet ns:dataset-
|
1024
|
+
qb:dataSet ns:dataset-MAF_ah1iit ;
|
1029
1025
|
prop:Variant_Classification <code/variant_classification/Missense_Mutation> ;
|
1030
1026
|
prop:Variant_Type <code/variant_type/SNP> ;
|
1031
1027
|
prop:dbSNP_Val_Status <code/dbsnp_val_status/> ;
|
@@ -1061,7 +1057,7 @@ ns:obs4 a qb:Observation ;
|
|
1061
1057
|
.
|
1062
1058
|
|
1063
1059
|
ns:obs5 a qb:Observation ;
|
1064
|
-
qb:dataSet ns:dataset-
|
1060
|
+
qb:dataSet ns:dataset-MAF_ah1iit ;
|
1065
1061
|
prop:Variant_Classification <code/variant_classification/Silent> ;
|
1066
1062
|
prop:Variant_Type <code/variant_type/SNP> ;
|
1067
1063
|
prop:dbSNP_Val_Status <code/dbsnp_val_status/> ;
|
@@ -1097,7 +1093,7 @@ ns:obs5 a qb:Observation ;
|
|
1097
1093
|
.
|
1098
1094
|
|
1099
1095
|
ns:obs6 a qb:Observation ;
|
1100
|
-
qb:dataSet ns:dataset-
|
1096
|
+
qb:dataSet ns:dataset-MAF_ah1iit ;
|
1101
1097
|
prop:Variant_Classification <code/variant_classification/Silent> ;
|
1102
1098
|
prop:Variant_Type <code/variant_type/SNP> ;
|
1103
1099
|
prop:dbSNP_Val_Status <code/dbsnp_val_status/> ;
|
@@ -1132,7 +1128,7 @@ ns:obs6 a qb:Observation ;
|
|
1132
1128
|
.
|
1133
1129
|
|
1134
1130
|
ns:obs7 a qb:Observation ;
|
1135
|
-
qb:dataSet ns:dataset-
|
1131
|
+
qb:dataSet ns:dataset-MAF_ah1iit ;
|
1136
1132
|
prop:Variant_Classification <code/variant_classification/Missense_Mutation> ;
|
1137
1133
|
prop:Variant_Type <code/variant_type/SNP> ;
|
1138
1134
|
prop:dbSNP_Val_Status <code/dbsnp_val_status/> ;
|
@@ -1171,3 +1167,83 @@ ns:obs7 a qb:Observation ;
|
|
1171
1167
|
prop:sample_id "01A-11D-A14G-09" ;
|
1172
1168
|
.
|
1173
1169
|
|
1170
|
+
ns:obs8 a qb:Observation ;
|
1171
|
+
qb:dataSet ns:dataset-MAF_ah1iit ;
|
1172
|
+
prop:Variant_Classification <code/variant_classification/Silent> ;
|
1173
|
+
prop:Variant_Type <code/variant_type/SNP> ;
|
1174
|
+
prop:dbSNP_Val_Status <code/dbsnp_val_status/> ;
|
1175
|
+
prop:Verification_Status <code/verification_status/Unknown> ;
|
1176
|
+
prop:Validation_Status <code/validation_status/Valid> ;
|
1177
|
+
prop:Mutation_Status <code/mutation_status/Somatic> ;
|
1178
|
+
prop:Sequence_Source <code/sequence_source/WXS> ;
|
1179
|
+
prop:Sequencer <code/sequencer/Illumina_GAIIx> ;
|
1180
|
+
prop:Hugo_Symbol <http://identifiers.org/hgnc.symbol/A2BP1> ;
|
1181
|
+
prop:Entrez_Gene_Id <http://identifiers.org/ncbigene/54715> ;
|
1182
|
+
prop:Center "genome.wustl.edu" ;
|
1183
|
+
prop:NCBI_Build 37 ;
|
1184
|
+
prop:Chromosome 16 ;
|
1185
|
+
prop:Start_Position 7383011 ;
|
1186
|
+
prop:End_Position 7383011 ;
|
1187
|
+
prop:Strand "+" ;
|
1188
|
+
prop:Reference_Allele "G" ;
|
1189
|
+
prop:Tumor_Seq_Allele1 "G" ;
|
1190
|
+
prop:Tumor_Seq_Allele2 "A" ;
|
1191
|
+
prop:dbSNP_RS "novel" ;
|
1192
|
+
prop:Tumor_Sample_Barcode "TCGA-AR-A1AJ-01A-21D-A12Q-09" ;
|
1193
|
+
prop:Matched_Norm_Sample_Barcode "TCGA-AR-A1AJ-10A-01D-A12Q-09" ;
|
1194
|
+
prop:Match_Norm_Seq_Allele1 "G" ;
|
1195
|
+
prop:Match_Norm_Seq_Allele2 "G" ;
|
1196
|
+
prop:Tumor_Validation_Allele1 "G" ;
|
1197
|
+
prop:Tumor_Validation_Allele2 "A" ;
|
1198
|
+
prop:Match_Norm_Validation_Allele1 "G" ;
|
1199
|
+
prop:Match_Norm_Validation_Allele2 "G" ;
|
1200
|
+
prop:Sequencing_Phase "Phase_IV" ;
|
1201
|
+
prop:Validation_Method "Illumina_WXS_gDNA" ;
|
1202
|
+
prop:Score 1 ;
|
1203
|
+
prop:BAM_File "dbGAP" ;
|
1204
|
+
prop:Tumor_Sample_UUID "4e1f9084-4729-4b3f-b036-6226d64fd25b" ;
|
1205
|
+
prop:Matched_Norm_Sample_UUID "63ee3781-4578-4d19-88e4-c8785fc7987e" ;
|
1206
|
+
prop:patient_id "AR-A1AJ" ;
|
1207
|
+
prop:sample_id "01A-21D-A12Q-09" ;
|
1208
|
+
.
|
1209
|
+
|
1210
|
+
ns:obs9 a qb:Observation ;
|
1211
|
+
qb:dataSet ns:dataset-MAF_ah1iit ;
|
1212
|
+
prop:Variant_Classification <code/variant_classification/Nonsense_Mutation> ;
|
1213
|
+
prop:Variant_Type <code/variant_type/SNP> ;
|
1214
|
+
prop:dbSNP_Val_Status <code/dbsnp_val_status/> ;
|
1215
|
+
prop:Verification_Status <code/verification_status/Unknown> ;
|
1216
|
+
prop:Validation_Status <code/validation_status/Valid> ;
|
1217
|
+
prop:Mutation_Status <code/mutation_status/Somatic> ;
|
1218
|
+
prop:Sequence_Source <code/sequence_source/WXS> ;
|
1219
|
+
prop:Sequencer <code/sequencer/Illumina_GAIIx> ;
|
1220
|
+
prop:Hugo_Symbol <http://identifiers.org/hgnc.symbol/A2M> ;
|
1221
|
+
prop:Entrez_Gene_Id <http://identifiers.org/ncbigene/2> ;
|
1222
|
+
prop:Center "genome.wustl.edu" ;
|
1223
|
+
prop:NCBI_Build 37 ;
|
1224
|
+
prop:Chromosome 12 ;
|
1225
|
+
prop:Start_Position 9251298 ;
|
1226
|
+
prop:End_Position 9251298 ;
|
1227
|
+
prop:Strand "+" ;
|
1228
|
+
prop:Reference_Allele "G" ;
|
1229
|
+
prop:Tumor_Seq_Allele1 "G" ;
|
1230
|
+
prop:Tumor_Seq_Allele2 "A" ;
|
1231
|
+
prop:dbSNP_RS "novel" ;
|
1232
|
+
prop:Tumor_Sample_Barcode "TCGA-A8-A08G-01A-11W-A019-09" ;
|
1233
|
+
prop:Matched_Norm_Sample_Barcode "TCGA-A8-A08G-10A-01W-A021-09" ;
|
1234
|
+
prop:Match_Norm_Seq_Allele1 "G" ;
|
1235
|
+
prop:Match_Norm_Seq_Allele2 "G" ;
|
1236
|
+
prop:Tumor_Validation_Allele1 "G" ;
|
1237
|
+
prop:Tumor_Validation_Allele2 "A" ;
|
1238
|
+
prop:Match_Norm_Validation_Allele1 "G" ;
|
1239
|
+
prop:Match_Norm_Validation_Allele2 "G" ;
|
1240
|
+
prop:Sequencing_Phase "Phase_IV" ;
|
1241
|
+
prop:Validation_Method "Illumina_WXS_gDNA" ;
|
1242
|
+
prop:Score 1 ;
|
1243
|
+
prop:BAM_File "dbGAP" ;
|
1244
|
+
prop:Tumor_Sample_UUID "8da61928-e935-4a33-8e46-840e637163d7" ;
|
1245
|
+
prop:Matched_Norm_Sample_UUID "74a3a4af-c93a-4fcd-af11-1f5eeb847c3c" ;
|
1246
|
+
prop:patient_id "A8-A08G" ;
|
1247
|
+
prop:sample_id "01A-11W-A019-09" ;
|
1248
|
+
.
|
1249
|
+
|