{"@context":{"ns0":"http://www.biointerchange.org/gfvo#","rdf":"http://www.w3.org/1999/02/22-rdf-syntax-ns#","owl":"http://www.w3.org/2002/07/owl#","rdfs":"http://www.w3.org/2000/01/rdf-schema#","ns1":"http://samtools.github.io/hts-specs/","ns2":"http://sequenceontology.org/resources/","ns3":"http://www.1000genomes.org/wiki/Analysis/Variant%20Call%20Format/","ns4":"http://www.ensembl.org/info/website/upload/","metadata_def":"http://data.bioontology.org/metadata/def/","metadata":"http://data.bioontology.org/metadata/"},"@id":"ns0:Feature","@type":"owl:Class","rdfs:subClassOf":{"@id":"ns0:InformationContentEntity"},"rdfs:label":"Feature","rdfs:isDefinedBy":[{"@id":"ns1:VCFv4.2.pdf"},{"@id":"ns2:gvf.html"},{"@id":"ns3:vcf-variant-call-format-version-41"},{"@id":"ns4:gff.html"},{"@id":"ns1:VCFv4.1.pdf"},{"@id":"ns2:gff3.html"}],"rdfs:comment":{"@language":"en","@value":"The feature class captures information about genomic sequence features and variations. A genomic feature can be a large object, such as a chromosome or contig, down to single base-pair reference or variant alleles."},"metadata:def/prefLabel":"Feature","metadata:def/mappingLoom":"feature","metadata:def/mappingSameURI":{"@id":"ns0:Feature"},"metadata:prefixIRI":"Feature"}