@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:NP570760.RA5SnPFXlmh3hwJ4f2mB2H7S_fIAGGqecn1_BSn48Nsug130_head { this: np:hasAssertion dgn-np:NP570760.RA5SnPFXlmh3hwJ4f2mB2H7S_fIAGGqecn1_BSn48Nsug130_assertion; np:hasProvenance dgn-np:NP570760.RA5SnPFXlmh3hwJ4f2mB2H7S_fIAGGqecn1_BSn48Nsug130_provenance; np:hasPublicationInfo dgn-np:NP570760.RA5SnPFXlmh3hwJ4f2mB2H7S_fIAGGqecn1_BSn48Nsug130_publicationInfo; a np:Nanopublication . dgn-np:NP570760.RA5SnPFXlmh3hwJ4f2mB2H7S_fIAGGqecn1_BSn48Nsug130_assertion a np:Assertion . dgn-np:NP570760.RA5SnPFXlmh3hwJ4f2mB2H7S_fIAGGqecn1_BSn48Nsug130_provenance a np:Provenance . dgn-np:NP570760.RA5SnPFXlmh3hwJ4f2mB2H7S_fIAGGqecn1_BSn48Nsug130_publicationInfo a np:PublicationInfo . } dgn-np:NP570760.RA5SnPFXlmh3hwJ4f2mB2H7S_fIAGGqecn1_BSn48Nsug130_assertion { miriam-gene:4439 a ncit:C16612 . lld:C0024305 a ncit:C7057 . dgn-gda:DGN04f9a22b35e8fdb6783bf2725f1e4596 sio:SIO_000628 miriam-gene:4439, lld:C0024305; a sio:SIO_001122 . } dgn-np:NP570760.RA5SnPFXlmh3hwJ4f2mB2H7S_fIAGGqecn1_BSn48Nsug130_provenance { dgn-np:NP570760.RA5SnPFXlmh3hwJ4f2mB2H7S_fIAGGqecn1_BSn48Nsug130_assertion dcterms:description "[In the pleiotropy analysis, six risk variants for other cancers were associated with NHL risk, including variants for lung (rs401681 in TERT: OR per C allele=0.89, p=3.7 × E-03; rs4975616 in TERT: OR per A allele=0.90, p=0.01; rs3131379 in MSH5: OR per T allele=1.16, p=0.03), prostate (rs7679673 in TET2: OR per C allele=0.89, p=5.7 × E-03; rs10993994 in MSMB: OR per T allele=1.09, p=0.04), and breast (rs3817198 in LSP1: OR per C allele=1.12, p=0.01) cancers, but none of these associations remained significant after multiple test correction.]. 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:24598796; 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:NP570760.RA5SnPFXlmh3hwJ4f2mB2H7S_fIAGGqecn1_BSn48Nsug130_publicationInfo { this: dcterms:created "2015-08-25T14:43:19+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" . }