@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:NP429472.RAzuUc-Lcqdd4zpeiNm9YiB5PHUVDgj4ukipaFR7XAugc130_head { this: np:hasAssertion dgn-np:NP429472.RAzuUc-Lcqdd4zpeiNm9YiB5PHUVDgj4ukipaFR7XAugc130_assertion; np:hasProvenance dgn-np:NP429472.RAzuUc-Lcqdd4zpeiNm9YiB5PHUVDgj4ukipaFR7XAugc130_provenance; np:hasPublicationInfo dgn-np:NP429472.RAzuUc-Lcqdd4zpeiNm9YiB5PHUVDgj4ukipaFR7XAugc130_publicationInfo; a np:Nanopublication . dgn-np:NP429472.RAzuUc-Lcqdd4zpeiNm9YiB5PHUVDgj4ukipaFR7XAugc130_assertion a np:Assertion . dgn-np:NP429472.RAzuUc-Lcqdd4zpeiNm9YiB5PHUVDgj4ukipaFR7XAugc130_provenance a np:Provenance . dgn-np:NP429472.RAzuUc-Lcqdd4zpeiNm9YiB5PHUVDgj4ukipaFR7XAugc130_publicationInfo a np:PublicationInfo . } dgn-np:NP429472.RAzuUc-Lcqdd4zpeiNm9YiB5PHUVDgj4ukipaFR7XAugc130_assertion { miriam-gene:2776 a ncit:C16612 . lld:C0025202 a ncit:C7057 . dgn-gda:DGNa2549f4fd4efa2b60dd72e6bc349b180 sio:SIO_000628 miriam-gene:2776, lld:C0025202; a sio:SIO_001121 . } dgn-np:NP429472.RAzuUc-Lcqdd4zpeiNm9YiB5PHUVDgj4ukipaFR7XAugc130_provenance { dgn-np:NP429472.RAzuUc-Lcqdd4zpeiNm9YiB5PHUVDgj4ukipaFR7XAugc130_assertion dcterms:description "[The recent identification of frequent activating mutations in GNAQ or GNA11 in uveal melanoma provides an opportunity to better understand the pathogenesis of this melanoma subtype and to develop rational therapeutics to target the cellular effects mediated by these mutations.]. 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:22236444; prov:wasDerivedFrom dgn-void:befree-20150227; prov:wasGeneratedBy eco:ECO_0000203 . dgn-void:befree-20150227 pav:importedOn "2015-02-27"^^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:NP429472.RAzuUc-Lcqdd4zpeiNm9YiB5PHUVDgj4ukipaFR7XAugc130_publicationInfo { this: dcterms:created "2015-08-25T14:41:50+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" . }