@prefix rdf: <http://www.w3.org/1999/02/22-rdf-syntax-ns#> .
@prefix ns0: <http://www.biointerchange.org/gfvo#> .
@prefix owl: <http://www.w3.org/2002/07/owl#> .
@prefix rdfs: <http://www.w3.org/2000/01/rdf-schema#> .
@prefix ns1: <http://samtools.github.io/hts-specs/> .
@prefix ns2: <http://www.1000genomes.org/wiki/Analysis/Variant%20Call%20Format/> .
@prefix metadata_def: <http://data.bioontology.org/metadata/def/> .
@prefix metadata: <http://data.bioontology.org/metadata/> .
ns0:Haplotype
metadata_def:mappingLoom "haplotype" ;
metadata_def:mappingSameURI ns0:Haplotype ;
metadata_def:prefLabel "Haplotype" ;
metadata:prefixIRI "Haplotype" ;
a owl:Class ;
rdfs:comment """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).
Haplotype instances should only catalog a single type, i.e. either \"Genotype\" or \"Sequence Variant\" instances; they should not mix both types (see also \"Catalog\").
Encodes for \"HQ\" additional information in VCF."""@en ;
rdfs:isDefinedBy <http://samtools.github.io/hts-specs/VCFv4.1.pdf>, <http://samtools.github.io/hts-specs/VCFv4.2.pdf>, ns2:vcf-variant-call-format-version-41 ;
rdfs:label "Haplotype" ;
rdfs:seeAlso "http://en.wikipedia.org/wiki/Haplotype" ;
rdfs:subClassOf ns0:Catalog .
@prefix rdf: <http://www.w3.org/1999/02/22-rdf-syntax-ns#> .
@prefix ns0: <http://www.biointerchange.org/gfvo#> .
@prefix owl: <http://www.w3.org/2002/07/owl#> .
@prefix rdfs: <http://www.w3.org/2000/01/rdf-schema#> .
@prefix ns1: <http://samtools.github.io/hts-specs/> .
@prefix ns2: <http://www.1000genomes.org/wiki/Analysis/Variant%20Call%20Format/> .
@prefix metadata_def: <http://data.bioontology.org/metadata/def/> .
@prefix metadata: <http://data.bioontology.org/metadata/> .
ns0:Haplotype
metadata_def:mappingLoom "haplotype" ;
metadata_def:mappingSameURI ns0:Haplotype ;
metadata_def:prefLabel "Haplotype" ;
metadata:prefixIRI "Haplotype" ;
a owl:Class ;
rdfs:comment """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).
Haplotype instances should only catalog a single type, i.e. either \"Genotype\" or \"Sequence Variant\" instances; they should not mix both types (see also \"Catalog\").
Encodes for \"HQ\" additional information in VCF."""@en ;
rdfs:isDefinedBy <http://samtools.github.io/hts-specs/VCFv4.1.pdf>, <http://samtools.github.io/hts-specs/VCFv4.2.pdf>, ns2:vcf-variant-call-format-version-41 ;
rdfs:label "Haplotype" ;
rdfs:seeAlso "http://en.wikipedia.org/wiki/Haplotype" ;
rdfs:subClassOf ns0:Catalog .