<?xml version="1.0" encoding="UTF-8"?>
<rdf:RDF xmlns:rdf="http://www.w3.org/1999/02/22-rdf-syntax-ns#" xmlns:ns0="http://www.biointerchange.org/gfvo#" xmlns:owl="http://www.w3.org/2002/07/owl#" xmlns:rdfs="http://www.w3.org/2000/01/rdf-schema#" xmlns:ns1="http://samtools.github.io/hts-specs/" xmlns:ns2="http://www.1000genomes.org/wiki/Analysis/Variant%20Call%20Format/" xmlns:metadata_def="http://data.bioontology.org/metadata/def/" xmlns:metadata="http://data.bioontology.org/metadata/">
<owl:Class rdf:about="http://www.biointerchange.org/gfvo#Haplotype">
<rdfs:subClassOf rdf:resource="http://www.biointerchange.org/gfvo#Catalog"/>
<rdfs:label>Haplotype</rdfs:label>
<rdfs:isDefinedBy rdf:resource="http://samtools.github.io/hts-specs/VCFv4.2.pdf"/>
<rdfs:isDefinedBy rdf:resource="http://www.1000genomes.org/wiki/Analysis/Variant%20Call%20Format/vcf-variant-call-format-version-41"/>
<rdfs:isDefinedBy rdf:resource="http://samtools.github.io/hts-specs/VCFv4.1.pdf"/>
<rdfs:comment xml:lang="en">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.</rdfs:comment>
<rdfs:seeAlso>http://en.wikipedia.org/wiki/Haplotype</rdfs:seeAlso>
<metadata_def:prefLabel>Haplotype</metadata_def:prefLabel>
<metadata_def:mappingLoom>haplotype</metadata_def:mappingLoom>
<metadata_def:mappingSameURI rdf:resource="http://www.biointerchange.org/gfvo#Haplotype"/>
<metadata:prefixIRI>Haplotype</metadata:prefixIRI>
</owl:Class>
<rdf:Description rdf:about="http://www.biointerchange.org/gfvo#Haplotype">
<metadata_def:mappingSameURI rdf:resource="http://www.biointerchange.org/gfvo#Haplotype"/>
</rdf:Description>
</rdf:RDF>
<?xml version="1.0" encoding="UTF-8"?>
<rdf:RDF xmlns:rdf="http://www.w3.org/1999/02/22-rdf-syntax-ns#" xmlns:ns0="http://www.biointerchange.org/gfvo#" xmlns:owl="http://www.w3.org/2002/07/owl#" xmlns:rdfs="http://www.w3.org/2000/01/rdf-schema#" xmlns:ns1="http://samtools.github.io/hts-specs/" xmlns:ns2="http://www.1000genomes.org/wiki/Analysis/Variant%20Call%20Format/" xmlns:metadata_def="http://data.bioontology.org/metadata/def/" xmlns:metadata="http://data.bioontology.org/metadata/">
<owl:Class rdf:about="http://www.biointerchange.org/gfvo#Haplotype">
<rdfs:subClassOf rdf:resource="http://www.biointerchange.org/gfvo#Catalog"/>
<rdfs:label>Haplotype</rdfs:label>
<rdfs:isDefinedBy rdf:resource="http://samtools.github.io/hts-specs/VCFv4.2.pdf"/>
<rdfs:isDefinedBy rdf:resource="http://www.1000genomes.org/wiki/Analysis/Variant%20Call%20Format/vcf-variant-call-format-version-41"/>
<rdfs:isDefinedBy rdf:resource="http://samtools.github.io/hts-specs/VCFv4.1.pdf"/>
<rdfs:comment xml:lang="en">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.</rdfs:comment>
<rdfs:seeAlso>http://en.wikipedia.org/wiki/Haplotype</rdfs:seeAlso>
<metadata_def:prefLabel>Haplotype</metadata_def:prefLabel>
<metadata_def:mappingLoom>haplotype</metadata_def:mappingLoom>
<metadata_def:mappingSameURI rdf:resource="http://www.biointerchange.org/gfvo#Haplotype"/>
<metadata:prefixIRI>Haplotype</metadata:prefixIRI>
</owl:Class>
<rdf:Description rdf:about="http://www.biointerchange.org/gfvo#Haplotype">
<metadata_def:mappingSameURI rdf:resource="http://www.biointerchange.org/gfvo#Haplotype"/>
</rdf:Description>
</rdf:RDF>