{"@context":{"ns0":"http://www.loria.fr/~coulet/ontology/snpontology/version1.6/snpontology_full.owl#","rdf":"http://www.w3.org/1999/02/22-rdf-syntax-ns#","owl":"http://www.w3.org/2002/07/owl#","rdfs":"http://www.w3.org/2000/01/rdf-schema#","metadata_def":"http://data.bioontology.org/metadata/def/","metadata":"http://data.bioontology.org/metadata/"},"@graph":[{"@id":"ns0:variant","@type":"owl:Class","rdfs:subClassOf":{"@id":"owl:Thing"},"metadata:def/mappingSameURI":{"@id":"ns0:variant"},"metadata:def/mappingLoom":"variant","metadata:def/prefLabel":"variant","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.","metadata:prefixIRI":"SNPO:variant"},{"@id":"ns0:non_coding_variant","rdfs:subClassOf":{"@id":"ns0:variant"}},{"@id":"ns0:reference_variant","rdfs:subClassOf":{"@id":"ns0:variant"}},{"@id":"ns0:regionHasVariant","rdfs:range":{"@id":"ns0:variant"}},{"@id":"ns0:isNucleotideVariationOf","rdfs:range":{"@id":"ns0:variant"}},{"@id":"ns0:isAAVariationOf","rdfs:range":{"@id":"ns0:variant"}},{"@id":"ns0:haplotype_member","rdfs:subClassOf":{"@id":"ns0:variant"}},{"@id":"ns0:sequence","owl:disjointWith":{"@id":"ns0:variant"}},{"@id":"ns0:observed_variation","owl:disjointWith":{"@id":"ns0:variant"}},{"@id":"ns0:storesVariant","rdfs:range":{"@id":"ns0:variant"}},{"@id":"ns0:hasVariant","rdfs:range":{"@id":"ns0:variant"}},{"@id":"ns0:isVariantIn","rdfs:domain":{"@id":"ns0:variant"}},{"@id":"ns0:hasPosition","rdfs:domain":{"@id":"ns0:variant"}},{"@id":"ns0:uncaptured_snp","rdfs:subClassOf":{"@id":"ns0:variant"}},{"@id":"ns0:sequence_position","owl:disjointWith":{"@id":"ns0:variant"}},{"@id":"ns0:isObservedIn","rdfs:range":{"@id":"ns0:variant"}},{"@id":"ns0:isStoredInVarDb","rdfs:domain":{"@id":"ns0:variant"}},{"@id":"ns0:hasAAVariation","rdfs:domain":{"@id":"ns0:variant"}},{"@id":"ns0:coding_variant","rdfs:subClassOf":{"@id":"ns0:variant"}},{"@id":"ns0:database","owl:disjointWith":{"@id":"ns0:variant"}},{"@id":"ns0:hasNucleotideVariation","rdfs:domain":{"@id":"ns0:variant"}},{"@id":"ns0:identifierInRelatedVarDb","rdfs:domain":{"@id":"ns0:variant"}},{"@id":"ns0:hasVariation","rdfs:domain":{"@id":"ns0:variant"}}]}