@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 .