@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:reference_variant
metadata_def:mappingLoom "referencevariant" ;
metadata_def:mappingSameURI ns0:reference_variant ;
metadata_def:prefLabel "reference_variant" ;
metadata:prefixIRI "SNPO:reference_variant" ;
a owl:Class ;
rdfs:comment """Because one genomic variation could be represented in diferrent way (e.g. positionnned on different sequence, represented at the nucleotide or proteic level, etc.), several variant may refer to the same entity ; tit is interesting to have a reference variant. In our point of view, the reference variant is the one described at the genomic level on the complete chromosome sequence (of the current genome assembly).
Ex: on the NC_000019.8 sequence""" ;
rdfs:subClassOf ns0:variant .
@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:reference_variant
metadata_def:mappingLoom "referencevariant" ;
metadata_def:mappingSameURI ns0:reference_variant ;
metadata_def:prefLabel "reference_variant" ;
metadata:prefixIRI "SNPO:reference_variant" ;
a owl:Class ;
rdfs:comment """Because one genomic variation could be represented in diferrent way (e.g. positionnned on different sequence, represented at the nucleotide or proteic level, etc.), several variant may refer to the same entity ; tit is interesting to have a reference variant. In our point of view, the reference variant is the one described at the genomic level on the complete chromosome sequence (of the current genome assembly).
Ex: on the NC_000019.8 sequence""" ;
rdfs:subClassOf ns0:variant .