{"@context":{"obo_purl":"http://purl.obolibrary.org/obo/","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#","skos":"http://www.w3.org/2004/02/skos/core#","metadata_def":"http://data.bioontology.org/metadata/def/","oboinowl_gen":"http://www.geneontology.org/formats/oboInOwl#"},"@graph":[{"@id":"obo_purl:SO_0001878","@type":"owl:Class","rdfs:subClassOf":{"@id":"obo_purl:SO_0001537"},"skos:notation":"SO:0001878","metadata_def:mappingSameURI":{"@id":"obo_purl:SO_0001878"},"metadata_def:mappingLoom":"featurevariant","metadata_def:prefLabel":"feature_variant","rdfs:comment":"Created in conjunction with the EBI.","oboinowl_gen:creation_date":"2012-04-03T11:27:27Z","obo_purl:IAO_0000115":"A sequence variant that falls entirely or partially within a genomic feature.","oboinowl_gen:hasExactSynonym":"feature alteration","oboinowl_gen:hasOBONamespace":"sequence","oboinowl_gen:created_by":"kareneilbeck","rdfs:label":"feature_variant","oboinowl_gen:id":"SO:0001878"},{"@id":"obo_purl:SO_0001564","rdfs:subClassOf":{"@id":"obo_purl:SO_0001878"}},{"@id":"obo_purl:SO_0001628","rdfs:subClassOf":{"@id":"obo_purl:SO_0001878"}},{"@id":"obo_purl:SO_0001566","rdfs:subClassOf":{"@id":"obo_purl:SO_0001878"}},{"@id":"obo_purl:SO_0001017","rdfs:subClassOf":{"@id":"obo_purl:SO_0001878"}},{"@id":"obo_purl:SO_0001907","rdfs:subClassOf":{"@id":"obo_purl:SO_0001878"}},{"@id":"obo_purl:SO_0001906","rdfs:subClassOf":{"@id":"obo_purl:SO_0001878"}}]}