@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:NP76403.RAKxnptGFUZxYXPP7pP9IKn8AwDi_9-7B-DHGrZbeO7wE130_head { this: np:hasAssertion dgn-np:NP76403.RAKxnptGFUZxYXPP7pP9IKn8AwDi_9-7B-DHGrZbeO7wE130_assertion; np:hasProvenance dgn-np:NP76403.RAKxnptGFUZxYXPP7pP9IKn8AwDi_9-7B-DHGrZbeO7wE130_provenance; np:hasPublicationInfo dgn-np:NP76403.RAKxnptGFUZxYXPP7pP9IKn8AwDi_9-7B-DHGrZbeO7wE130_publicationInfo; a np:Nanopublication . dgn-np:NP76403.RAKxnptGFUZxYXPP7pP9IKn8AwDi_9-7B-DHGrZbeO7wE130_assertion a np:Assertion . dgn-np:NP76403.RAKxnptGFUZxYXPP7pP9IKn8AwDi_9-7B-DHGrZbeO7wE130_provenance a np:Provenance . dgn-np:NP76403.RAKxnptGFUZxYXPP7pP9IKn8AwDi_9-7B-DHGrZbeO7wE130_publicationInfo a np:PublicationInfo . } dgn-np:NP76403.RAKxnptGFUZxYXPP7pP9IKn8AwDi_9-7B-DHGrZbeO7wE130_assertion { miriam-gene:7517 a ncit:C16612 . lld:C0023418 a ncit:C7057 . dgn-gda:DGN49f3e3615fe9983b3874258d1b98401f sio:SIO_000628 miriam-gene:7517, lld:C0023418; a sio:SIO_001122 . } dgn-np:NP76403.RAKxnptGFUZxYXPP7pP9IKn8AwDi_9-7B-DHGrZbeO7wE130_provenance { dgn-np:NP76403.RAKxnptGFUZxYXPP7pP9IKn8AwDi_9-7B-DHGrZbeO7wE130_assertion dcterms:description "[Among the many comparisons, few polymorphisms were associated with the diseases at the univariate analysis: XRCC1-399 Gln/Gln variant homozygotes odds ratios (OR) = 2.20, 95% confidence intervals (CI) = 1.16-4.17 and XRCC3-241 Met/Met homozygotes (OR = 0.51, 95% CI = 0.27-0.96) and leukaemia.]. 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:16308313; prov:wasDerivedFrom dgn-void:gad-20150221; prov:wasGeneratedBy eco:ECO_0000203 . dgn-void:gad-20150221 pav:importedOn "2015-02-21"^^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:NP76403.RAKxnptGFUZxYXPP7pP9IKn8AwDi_9-7B-DHGrZbeO7wE130_publicationInfo { this: dcterms:created "2015-08-25T14:38:21+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" . }