{"@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/"},"@id":"ns0:Contig","@type":"owl:Class","rdfs:subClassOf":{"@id":"ns0:Collection"},"rdfs:label":"Contig","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":"A contig is a contiguous DNA sequence that has been assembled from shorter overlapping DNA segments. \"Contig\" is a specialization of a \"Collection\" and should be used to aggregate features, but not for indicating that a \"Landmark\" is representing a contig. It is encouraged that the latter is annotated by a term of the Sequence Ontology.\n\nEncodes for \"sequencing-scope\" in GVF and the \"contig\" information field in VCF."},"rdfs:seeAlso":"http://en.wikipedia.org/wiki/Contig","metadata:def/prefLabel":"Contig","metadata:def/mappingLoom":"contig","metadata:def/mappingSameURI":{"@id":"ns0:Contig"},"metadata:prefixIRI":"Contig"}