{"@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://www.1000genomes.org/wiki/Analysis/Variant%20Call%20Format/","metadata_def":"http://data.bioontology.org/metadata/def/","metadata":"http://data.bioontology.org/metadata/"},"@id":"ns0:Haplotype","@type":"owl:Class","rdfs:subClassOf":{"@id":"ns0:Catalog"},"rdfs:label":"Haplotype","rdfs:isDefinedBy":[{"@id":"ns1:VCFv4.2.pdf"},{"@id":"ns2:vcf-variant-call-format-version-41"},{"@id":"ns1:VCFv4.1.pdf"}],"rdfs:comment":{"@language":"en","@value":"A \"Haplotype\" is a collection of \"Genotype\" or \"Sequence Variant\" instances. It can imply that a set of genes is inherited as a group, or alternatively, that the set of genotypes or sequence variance has a biological function when acting together (e.g., there exists a disease association).\n\nHaplotype instances should only catalog a single type, i.e. either \"Genotype\" or \"Sequence Variant\" instances; they should not mix both types (see also \"Catalog\").\n\nEncodes for \"HQ\" additional information in VCF."},"rdfs:seeAlso":"http://en.wikipedia.org/wiki/Haplotype","metadata:def/prefLabel":"Haplotype","metadata:def/mappingLoom":"haplotype","metadata:def/mappingSameURI":{"@id":"ns0:Haplotype"},"metadata:prefixIRI":"Haplotype"}