@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:NP53599.RAgpN_xkPNaAE71fD4NmvWMG-e1X9SjDOSpMzjJHvdBgg130_head { this: np:hasAssertion dgn-np:NP53599.RAgpN_xkPNaAE71fD4NmvWMG-e1X9SjDOSpMzjJHvdBgg130_assertion; np:hasProvenance dgn-np:NP53599.RAgpN_xkPNaAE71fD4NmvWMG-e1X9SjDOSpMzjJHvdBgg130_provenance; np:hasPublicationInfo dgn-np:NP53599.RAgpN_xkPNaAE71fD4NmvWMG-e1X9SjDOSpMzjJHvdBgg130_publicationInfo; a np:Nanopublication . dgn-np:NP53599.RAgpN_xkPNaAE71fD4NmvWMG-e1X9SjDOSpMzjJHvdBgg130_assertion a np:Assertion . dgn-np:NP53599.RAgpN_xkPNaAE71fD4NmvWMG-e1X9SjDOSpMzjJHvdBgg130_provenance a np:Provenance . dgn-np:NP53599.RAgpN_xkPNaAE71fD4NmvWMG-e1X9SjDOSpMzjJHvdBgg130_publicationInfo a np:PublicationInfo . } dgn-np:NP53599.RAgpN_xkPNaAE71fD4NmvWMG-e1X9SjDOSpMzjJHvdBgg130_assertion { miriam-gene:51750 a ncit:C16612 . lld:C0017638 a ncit:C7057 . dgn-gda:DGN3bb3d89593da123ef921896d946ee4b5 sio:SIO_000628 miriam-gene:51750, lld:C0017638; a sio:SIO_001122 . } dgn-np:NP53599.RAgpN_xkPNaAE71fD4NmvWMG-e1X9SjDOSpMzjJHvdBgg130_provenance { dgn-np:NP53599.RAgpN_xkPNaAE71fD4NmvWMG-e1X9SjDOSpMzjJHvdBgg130_assertion dcterms:description "[We conducted a new independent GWAS of glioma using 1,856 cases and 4,955 controls (from 14 cohort studies, 3 case-control studies, and 1 population-based case-only study) and found evidence of strong replication for three of the seven previously reported associations at 20q13.33 (RTEL), 5p15.33 (TERT), and 9p21.3 (CDKN2BAS), and consistent association signals for the remaining four at 7p11.2 (EGFR both loci), 8q24.21 (CCDC26) and 11q23.3 (PHLDB1).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en; wi:evidence dgn-void:source_evidence_curated; sio:SIO_000772 miriam-pubmed:22886559; prov:wasDerivedFrom dgn-void:gwascat-2016; prov:wasGeneratedBy eco:ECO_0000218 . dgn-void:gwascat-2016 pav:importedOn "2016-01-27"^^xsd:date . dgn-void:source_evidence_curated a eco:ECO_0000205; rdfs:comment "Gene-disease associations manually curated."@en; rdfs:label "DisGeNET evidence - CURATED"@en . } dgn-np:NP53599.RAgpN_xkPNaAE71fD4NmvWMG-e1X9SjDOSpMzjJHvdBgg130_publicationInfo { this: dcterms:created "2016-05-13T12:42:12+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 "v4.0.0.0" . dgn-void:disgenetv3.0rdf pav:version "v4.0.0" . }