@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:NP673984.RAnWx76V7HlS9ut0yd18jyz3WAGW_1B4OhcVmZVQNY3EA130_head { this: np:hasAssertion dgn-np:NP673984.RAnWx76V7HlS9ut0yd18jyz3WAGW_1B4OhcVmZVQNY3EA130_assertion; np:hasProvenance dgn-np:NP673984.RAnWx76V7HlS9ut0yd18jyz3WAGW_1B4OhcVmZVQNY3EA130_provenance; np:hasPublicationInfo dgn-np:NP673984.RAnWx76V7HlS9ut0yd18jyz3WAGW_1B4OhcVmZVQNY3EA130_publicationInfo; a np:Nanopublication . dgn-np:NP673984.RAnWx76V7HlS9ut0yd18jyz3WAGW_1B4OhcVmZVQNY3EA130_assertion a np:Assertion . dgn-np:NP673984.RAnWx76V7HlS9ut0yd18jyz3WAGW_1B4OhcVmZVQNY3EA130_provenance a np:Provenance . dgn-np:NP673984.RAnWx76V7HlS9ut0yd18jyz3WAGW_1B4OhcVmZVQNY3EA130_publicationInfo a np:PublicationInfo . } dgn-np:NP673984.RAnWx76V7HlS9ut0yd18jyz3WAGW_1B4OhcVmZVQNY3EA130_assertion { miriam-gene:1636 a ncit:C16612 . lld:C0948008 a ncit:C7057 . dgn-gda:DGNc02ff7aca6cae855e5e8466d40e09e68 sio:SIO_000628 miriam-gene:1636, lld:C0948008; a sio:SIO_001122 . } dgn-np:NP673984.RAnWx76V7HlS9ut0yd18jyz3WAGW_1B4OhcVmZVQNY3EA130_provenance { dgn-np:NP673984.RAnWx76V7HlS9ut0yd18jyz3WAGW_1B4OhcVmZVQNY3EA130_assertion dcterms:description "[Among the gene polymorphisms tested in the study, association of gene polymorphisms with increasing risk of ischemic stroke was confirmed in 6 polymorphisms including angiotensin-converting enzyme insertion/deletion (ACE I/D; OR = 1.87, 95% CI = 1.45-2.42), methylenetetrahydrofolate reductase (MTHFR) C677T (OR = 1.55, 95% CI = 1.26-1.90), plasminogen activator inhibitor 1 (PAI-1) 4G/5G (OR = 1.79, 95% CI = 1.20-2.67), beta-fibrinogen (beta-Fg) -455A/G (OR = 1.48, 95% CI = 1.14-1.92), beta-Fg -148T/C (OR = 1.72, 95% CI = 1.42-2.07), apolipoprotein E (ApoE) epsilon2-4 (OR = 2.39, 95% CI = 1.94-2.95).]. 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:18511872; 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:NP673984.RAnWx76V7HlS9ut0yd18jyz3WAGW_1B4OhcVmZVQNY3EA130_publicationInfo { this: dcterms:created "2016-05-13T12:46:50+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" . }