@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:NP838578.RAGqzwu3QVDMjPeHGygr6I9hWNtAhKSPAq329o3_sGS_w130_head { this: np:hasAssertion dgn-np:NP838578.RAGqzwu3QVDMjPeHGygr6I9hWNtAhKSPAq329o3_sGS_w130_assertion; np:hasProvenance dgn-np:NP838578.RAGqzwu3QVDMjPeHGygr6I9hWNtAhKSPAq329o3_sGS_w130_provenance; np:hasPublicationInfo dgn-np:NP838578.RAGqzwu3QVDMjPeHGygr6I9hWNtAhKSPAq329o3_sGS_w130_publicationInfo; a np:Nanopublication . dgn-np:NP838578.RAGqzwu3QVDMjPeHGygr6I9hWNtAhKSPAq329o3_sGS_w130_assertion a np:Assertion . dgn-np:NP838578.RAGqzwu3QVDMjPeHGygr6I9hWNtAhKSPAq329o3_sGS_w130_provenance a np:Provenance . dgn-np:NP838578.RAGqzwu3QVDMjPeHGygr6I9hWNtAhKSPAq329o3_sGS_w130_publicationInfo a np:PublicationInfo . } dgn-np:NP838578.RAGqzwu3QVDMjPeHGygr6I9hWNtAhKSPAq329o3_sGS_w130_assertion { miriam-gene:10215 a ncit:C16612 . lld:C0029421 a ncit:C7057 . dgn-gda:DGN8938be18585cb79ac36aabdad4f68504 sio:SIO_000628 miriam-gene:10215, lld:C0029421; a sio:SIO_001122 . } dgn-np:NP838578.RAGqzwu3QVDMjPeHGygr6I9hWNtAhKSPAq329o3_sGS_w130_provenance { dgn-np:NP838578.RAGqzwu3QVDMjPeHGygr6I9hWNtAhKSPAq329o3_sGS_w130_assertion dcterms:description "[Five SNPs achieved 0.004 (the nominal p-value expected by chance), 3 with empirical significant p-values (rs10070190 (CDH9) p = 1 × 10(-3), rs4825476 (GRIA3) p = 4 × 10(-4), and rs1074815 (TPH2) p = 8 × 10(-4)) and 2 additional polymorphisms showing nominal significance (rs2834070 (OLIG2) p = 2 × 10(-3) and rs11783752 (SCL18A1) p = 3 × 10(-3)), were found to be related to both AN and OCD.]. 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:23337130; 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:NP838578.RAGqzwu3QVDMjPeHGygr6I9hWNtAhKSPAq329o3_sGS_w130_publicationInfo { this: dcterms:created "2015-08-25T14:46:09+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" . }