@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:NP1017382.RA8fNYBBjoLRf812VQG-vWEotQ8rFffI3jeQuxLN_8pD4130_head { this: np:hasAssertion dgn-np:NP1017382.RA8fNYBBjoLRf812VQG-vWEotQ8rFffI3jeQuxLN_8pD4130_assertion; np:hasProvenance dgn-np:NP1017382.RA8fNYBBjoLRf812VQG-vWEotQ8rFffI3jeQuxLN_8pD4130_provenance; np:hasPublicationInfo dgn-np:NP1017382.RA8fNYBBjoLRf812VQG-vWEotQ8rFffI3jeQuxLN_8pD4130_publicationInfo; a np:Nanopublication . dgn-np:NP1017382.RA8fNYBBjoLRf812VQG-vWEotQ8rFffI3jeQuxLN_8pD4130_assertion a np:Assertion . dgn-np:NP1017382.RA8fNYBBjoLRf812VQG-vWEotQ8rFffI3jeQuxLN_8pD4130_provenance a np:Provenance . dgn-np:NP1017382.RA8fNYBBjoLRf812VQG-vWEotQ8rFffI3jeQuxLN_8pD4130_publicationInfo a np:PublicationInfo . } dgn-np:NP1017382.RA8fNYBBjoLRf812VQG-vWEotQ8rFffI3jeQuxLN_8pD4130_assertion { miriam-gene:7157 a ncit:C16612 . lld:C0026764 a ncit:C7057 . dgn-gda:DGN13f33ed8201cc2e65906407f6206f49a sio:SIO_000628 miriam-gene:7157, lld:C0026764; a sio:SIO_001122 . } dgn-np:NP1017382.RA8fNYBBjoLRf812VQG-vWEotQ8rFffI3jeQuxLN_8pD4130_provenance { dgn-np:NP1017382.RA8fNYBBjoLRf812VQG-vWEotQ8rFffI3jeQuxLN_8pD4130_assertion dcterms:description "[Through searching PubMed databases (or hand searching) up to April 2012 using the following MeSH terms and keywords: p53, codon 72 polymorphism and leukemia, or lymphoma, or myeloma, thirteen were identified as eligible articles in this meta-analysis for p53 Arg72Pro polymorphism (2,731 cases and 7, 356 controls), including nine studies on leukemia (1,266 cases and 4, 474 controls), three studies on lymphoma (1,359 cases and 2,652 controls), and one study on myeloma.]. 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:23029260; prov:wasDerivedFrom dgn-void:befree-2016; prov:wasGeneratedBy eco:ECO_0000203 . dgn-void:befree-2016 pav:importedOn "2016-02-19"^^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:NP1017382.RA8fNYBBjoLRf812VQG-vWEotQ8rFffI3jeQuxLN_8pD4130_publicationInfo { this: dcterms:created "2016-05-13T12:49:27+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" . }