{"@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:observed_variation","@type":"owl:Class","rdfs:subClassOf":{"@id":"owl:Thing"},"metadata:def/mappingSameURI":{"@id":"ns0:observed_variation"},"metadata:def/mappingLoom":"observedvariation","owl:disjointWith":[{"@id":"ns0:sequence"},{"@id":"ns0:sequence_position"},{"@id":"ns0:variant"}],"metadata:def/prefLabel":"observed_variation","rdfs:comment":"It is the variation (of nucleotides or of residues) observed between the 2 patients (reference sequence and the alternative sequence - if it's possible to talk about a \"reference\") when a genomic variation is described. \nEx: A>C, CT>A, Ser>Thr, etc.","metadata:prefixIRI":"SNPO:observed_variation"},{"@id":"ns0:nucleotide_variation","rdfs:subClassOf":{"@id":"ns0:observed_variation"}},{"@id":"ns0:isOneObservedAlleleIn","rdfs:range":{"@id":"ns0:observed_variation"}},{"@id":"ns0:hasVariantAASequence","rdfs:domain":{"@id":"ns0:observed_variation"}},{"@id":"ns0:hasVariantAlleleSequence","rdfs:domain":{"@id":"ns0:observed_variation"}},{"@id":"ns0:aa_variation","rdfs:subClassOf":{"@id":"ns0:observed_variation"}},{"@id":"ns0:isOneObservedVariantIn","rdfs:range":{"@id":"ns0:observed_variation"}},{"@id":"ns0:isOneObservedAASequenceIn","rdfs:range":{"@id":"ns0:observed_variation"}},{"@id":"ns0:hasVariantSequence","rdfs:domain":{"@id":"ns0:observed_variation"}},{"@id":"ns0:database","owl:disjointWith":{"@id":"ns0:observed_variation"}}]}