{"@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/","metadata_def":"http://data.bioontology.org/metadata/def/","metadata":"http://data.bioontology.org/metadata/"},"@graph":[{"@id":"ns0:ReferenceSequence","@type":"owl:Class","rdfs:subClassOf":{"@id":"ns0:DNASequence"},"rdfs:label":"Reference Sequence","rdfs:isDefinedBy":[{"@id":"ns1:VCFv4.2.pdf"},{"@id":"ns2:gvf.html"},{"@id":"ns3:vcf-variant-call-format-version-41"},{"@id":"ns1:VCFv4.1.pdf"}],"rdfs:comment":{"@language":"en","@value":"Denotes the reference sequence of a feature. The reference sequence is of importance when dealing with genomic variation data, which is expressed by the \"Variant\" class.\n\nEncodes for the \"Reference_seq\" and \"Sequence_context\" attributes in GVF and the \"REF\" column in VCF."},"rdfs:seeAlso":"http://en.wikipedia.org/wiki/Reference_sequence","metadata:def/prefLabel":"Reference Sequence","metadata:def/mappingLoom":"referencesequence","metadata:def/mappingSameURI":{"@id":"ns0:ReferenceSequence"},"metadata:prefixIRI":"ReferenceSequence"},{"@id":"ns0:AncestralSequence","rdfs:subClassOf":{"@id":"ns0:ReferenceSequence"}}]}