@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:NP958610.RAvoY0mpgMt3T7mb_uy2L4LFHBC_y3A1yxXn3HLIUse_8130_head { this: np:hasAssertion dgn-np:NP958610.RAvoY0mpgMt3T7mb_uy2L4LFHBC_y3A1yxXn3HLIUse_8130_assertion; np:hasProvenance dgn-np:NP958610.RAvoY0mpgMt3T7mb_uy2L4LFHBC_y3A1yxXn3HLIUse_8130_provenance; np:hasPublicationInfo dgn-np:NP958610.RAvoY0mpgMt3T7mb_uy2L4LFHBC_y3A1yxXn3HLIUse_8130_publicationInfo; a np:Nanopublication . dgn-np:NP958610.RAvoY0mpgMt3T7mb_uy2L4LFHBC_y3A1yxXn3HLIUse_8130_assertion a np:Assertion . dgn-np:NP958610.RAvoY0mpgMt3T7mb_uy2L4LFHBC_y3A1yxXn3HLIUse_8130_provenance a np:Provenance . dgn-np:NP958610.RAvoY0mpgMt3T7mb_uy2L4LFHBC_y3A1yxXn3HLIUse_8130_publicationInfo a np:PublicationInfo . } dgn-np:NP958610.RAvoY0mpgMt3T7mb_uy2L4LFHBC_y3A1yxXn3HLIUse_8130_assertion { miriam-gene:84938 a ncit:C16612 . lld:C1306459 a ncit:C7057 . dgn-gda:DGNcd78fde7bf0e68c47f81b0ab17225873 sio:SIO_000628 miriam-gene:84938, lld:C1306459; a sio:SIO_001121 . } dgn-np:NP958610.RAvoY0mpgMt3T7mb_uy2L4LFHBC_y3A1yxXn3HLIUse_8130_provenance { dgn-np:NP958610.RAvoY0mpgMt3T7mb_uy2L4LFHBC_y3A1yxXn3HLIUse_8130_assertion dcterms:description "[These SNPs are in or near genes that are highly expressed in the brain (HECW2, HIP1, BIN2, GRIA1), genes involved in neural development and function (KCNQ4, LMO4, GRIA1, NETO1) and autophagy (ATG4C), and genes that are associated with risk of various diseases including cancer and Alzheimer's disease.]. 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:21782286; 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:NP958610.RAvoY0mpgMt3T7mb_uy2L4LFHBC_y3A1yxXn3HLIUse_8130_publicationInfo { this: dcterms:created "2015-08-25T14:47:25+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" . }