@prefix this: . @prefix rdfs: . @prefix xsd: . @prefix sio: . @prefix ncit: . @prefix lld: . @prefix miriam-gene: . @prefix miriam-pubmed: . @prefix eco: . @prefix wi: . @prefix prov: . @prefix pav: . @prefix prv: . @prefix dcterms: . @prefix np: . @prefix dgn-np: . @prefix dgn-gda: . @prefix dgn-void: . dgn-np:NP160311.RAGkTzx-7QPBU0OotvYZc0-j3wIXhGUG7ooIA4zRQtgZg130_head { this: np:hasAssertion dgn-np:NP160311.RAGkTzx-7QPBU0OotvYZc0-j3wIXhGUG7ooIA4zRQtgZg130_assertion; np:hasProvenance dgn-np:NP160311.RAGkTzx-7QPBU0OotvYZc0-j3wIXhGUG7ooIA4zRQtgZg130_provenance; np:hasPublicationInfo dgn-np:NP160311.RAGkTzx-7QPBU0OotvYZc0-j3wIXhGUG7ooIA4zRQtgZg130_publicationInfo; a np:Nanopublication . dgn-np:NP160311.RAGkTzx-7QPBU0OotvYZc0-j3wIXhGUG7ooIA4zRQtgZg130_assertion a np:Assertion . dgn-np:NP160311.RAGkTzx-7QPBU0OotvYZc0-j3wIXhGUG7ooIA4zRQtgZg130_provenance a np:Provenance . dgn-np:NP160311.RAGkTzx-7QPBU0OotvYZc0-j3wIXhGUG7ooIA4zRQtgZg130_publicationInfo a np:PublicationInfo . } dgn-np:NP160311.RAGkTzx-7QPBU0OotvYZc0-j3wIXhGUG7ooIA4zRQtgZg130_assertion { miriam-gene:5816 a ncit:C16612 . lld:C0033953 a ncit:C7057 . dgn-gda:DGN3a5c1c24b9bce461b58bd6bc1d28d653 sio:SIO_000628 miriam-gene:5816, lld:C0033953; a sio:SIO_001122 . } dgn-np:NP160311.RAGkTzx-7QPBU0OotvYZc0-j3wIXhGUG7ooIA4zRQtgZg130_provenance { dgn-np:NP160311.RAGkTzx-7QPBU0OotvYZc0-j3wIXhGUG7ooIA4zRQtgZg130_assertion dcterms:description "[We report the first GWAS of FSD symptoms in humans. This has pointed to several 'risk alleles' and the implication of the serotonin and GABA pathways. Ultimately, understanding key mechanisms via this research may lead to new FSD treatments and inform cli]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en; wi:evidence dgn-void:source_evidence_literature; sio:SIO_000772 miriam-pubmed:22509378; prov:wasDerivedFrom dgn-void:gad-20150221; prov:wasGeneratedBy eco:ECO_0000203 . dgn-void:gad-20150221 pav:importedOn "2015-02-21"^^xsd:date . dgn-void:source_evidence_literature a eco:ECO_0000212; rdfs:comment "Gene-disease associations inferred from text-mining the literature."@en; rdfs:label "DisGeNET evidence - LITERATURE"@en . } dgn-np:NP160311.RAGkTzx-7QPBU0OotvYZc0-j3wIXhGUG7ooIA4zRQtgZg130_publicationInfo { this: dcterms:created "2015-08-25T14:39:11+02:00"^^xsd:dateTime; dcterms:rights ; dcterms:rightsHolder dgn-void:IBIGroup; dcterms:subject sio:SIO_000983; prv:usedData dgn-void:disgenetv3.0rdf; pav:authoredBy , , , , ; pav:createdBy ; pav:version "v3.0.0.0" . dgn-void:disgenetv3.0rdf pav:version "v3.0.0" . }