@prefix rdf: <http://www.w3.org/1999/02/22-rdf-syntax-ns#> .
@prefix ns0: <http://www.loria.fr/~coulet/ontology/snpontology/version1.6/snpontology_full.owl#> .
@prefix owl: <http://www.w3.org/2002/07/owl#> .
@prefix rdfs: <http://www.w3.org/2000/01/rdf-schema#> .
@prefix metadata_def: <http://data.bioontology.org/metadata/def/> .
@prefix metadata: <http://data.bioontology.org/metadata/> .
ns0:coding_variant
rdfs:subClassOf ns0:variant .
ns0:database
owl:disjointWith ns0:variant .
ns0:haplotype_member
rdfs:subClassOf ns0:variant .
ns0:hasAAVariation
rdfs:domain ns0:variant .
ns0:hasNucleotideVariation
rdfs:domain ns0:variant .
ns0:hasPosition
rdfs:domain ns0:variant .
ns0:hasVariant
rdfs:range ns0:variant .
ns0:hasVariation
rdfs:domain ns0:variant .
ns0:identifierInRelatedVarDb
rdfs:domain ns0:variant .
ns0:isAAVariationOf
rdfs:range ns0:variant .
ns0:isNucleotideVariationOf
rdfs:range ns0:variant .
ns0:isObservedIn
rdfs:range ns0:variant .
ns0:isStoredInVarDb
rdfs:domain ns0:variant .
ns0:isVariantIn
rdfs:domain ns0:variant .
ns0:non_coding_variant
rdfs:subClassOf ns0:variant .
ns0:observed_variation
owl:disjointWith ns0:variant .
ns0:reference_variant
rdfs:subClassOf ns0:variant .
ns0:regionHasVariant
rdfs:range ns0:variant .
ns0:sequence
owl:disjointWith ns0:variant .
ns0:sequence_position
owl:disjointWith ns0:variant .
ns0:storesVariant
rdfs:range ns0:variant .
ns0:uncaptured_snp
rdfs:subClassOf ns0:variant .
ns0:variant
metadata_def:mappingLoom "variant" ;
metadata_def:mappingSameURI ns0:variant ;
metadata_def:prefLabel "variant" ;
metadata:prefixIRI "SNPO:variant" ;
a owl:Class ;
rdfs:comment "A variant is a genomic variation description at the nucleotide or proteic level. It is defined by a position on a sequence. This sequence could be either a nucleotide sequence if the observed variation is a nucleotide variation, either a residue change if the observed variation is an residue variation. At the precised position is observed a variation (the observed variation) in the sequence respectively to a \"reference\" (or \"known\") sequence." ;
rdfs:subClassOf owl:Thing .
@prefix rdf: <http://www.w3.org/1999/02/22-rdf-syntax-ns#> .
@prefix ns0: <http://www.loria.fr/~coulet/ontology/snpontology/version1.6/snpontology_full.owl#> .
@prefix owl: <http://www.w3.org/2002/07/owl#> .
@prefix rdfs: <http://www.w3.org/2000/01/rdf-schema#> .
@prefix metadata_def: <http://data.bioontology.org/metadata/def/> .
@prefix metadata: <http://data.bioontology.org/metadata/> .
ns0:coding_variant
rdfs:subClassOf ns0:variant .
ns0:database
owl:disjointWith ns0:variant .
ns0:haplotype_member
rdfs:subClassOf ns0:variant .
ns0:hasAAVariation
rdfs:domain ns0:variant .
ns0:hasNucleotideVariation
rdfs:domain ns0:variant .
ns0:hasPosition
rdfs:domain ns0:variant .
ns0:hasVariant
rdfs:range ns0:variant .
ns0:hasVariation
rdfs:domain ns0:variant .
ns0:identifierInRelatedVarDb
rdfs:domain ns0:variant .
ns0:isAAVariationOf
rdfs:range ns0:variant .
ns0:isNucleotideVariationOf
rdfs:range ns0:variant .
ns0:isObservedIn
rdfs:range ns0:variant .
ns0:isStoredInVarDb
rdfs:domain ns0:variant .
ns0:isVariantIn
rdfs:domain ns0:variant .
ns0:non_coding_variant
rdfs:subClassOf ns0:variant .
ns0:observed_variation
owl:disjointWith ns0:variant .
ns0:reference_variant
rdfs:subClassOf ns0:variant .
ns0:regionHasVariant
rdfs:range ns0:variant .
ns0:sequence
owl:disjointWith ns0:variant .
ns0:sequence_position
owl:disjointWith ns0:variant .
ns0:storesVariant
rdfs:range ns0:variant .
ns0:uncaptured_snp
rdfs:subClassOf ns0:variant .
ns0:variant
metadata_def:mappingLoom "variant" ;
metadata_def:mappingSameURI ns0:variant ;
metadata_def:prefLabel "variant" ;
metadata:prefixIRI "SNPO:variant" ;
a owl:Class ;
rdfs:comment "A variant is a genomic variation description at the nucleotide or proteic level. It is defined by a position on a sequence. This sequence could be either a nucleotide sequence if the observed variation is a nucleotide variation, either a residue change if the observed variation is an residue variation. At the precised position is observed a variation (the observed variation) in the sequence respectively to a \"reference\" (or \"known\") sequence." ;
rdfs:subClassOf owl:Thing .