@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:NP318726.RA2OsChAkADnbvb9kkuDP_s4frXPJwtO3p8I8Kt1KImQA130_head { this: np:hasAssertion dgn-np:NP318726.RA2OsChAkADnbvb9kkuDP_s4frXPJwtO3p8I8Kt1KImQA130_assertion; np:hasProvenance dgn-np:NP318726.RA2OsChAkADnbvb9kkuDP_s4frXPJwtO3p8I8Kt1KImQA130_provenance; np:hasPublicationInfo dgn-np:NP318726.RA2OsChAkADnbvb9kkuDP_s4frXPJwtO3p8I8Kt1KImQA130_publicationInfo; a np:Nanopublication . dgn-np:NP318726.RA2OsChAkADnbvb9kkuDP_s4frXPJwtO3p8I8Kt1KImQA130_assertion a np:Assertion . dgn-np:NP318726.RA2OsChAkADnbvb9kkuDP_s4frXPJwtO3p8I8Kt1KImQA130_provenance a np:Provenance . dgn-np:NP318726.RA2OsChAkADnbvb9kkuDP_s4frXPJwtO3p8I8Kt1KImQA130_publicationInfo a np:PublicationInfo . } dgn-np:NP318726.RA2OsChAkADnbvb9kkuDP_s4frXPJwtO3p8I8Kt1KImQA130_assertion { miriam-gene:1677 a ncit:C16612 . lld:C1956346 a ncit:C7057 . dgn-gda:DGNb1bf07d45ba4d851a48071fc3d7ec202 sio:SIO_000628 miriam-gene:1677, lld:C1956346; a sio:SIO_001122 . } dgn-np:NP318726.RA2OsChAkADnbvb9kkuDP_s4frXPJwtO3p8I8Kt1KImQA130_provenance { dgn-np:NP318726.RA2OsChAkADnbvb9kkuDP_s4frXPJwtO3p8I8Kt1KImQA130_assertion dcterms:description "[We determined the prevalence of the G20210A mutation and prothrombin activity in 660 individuals, of whom 436 had angiographically documented severe coronary artery disease (CAD patients) and 224 had normal coronary angiography (CAD-free control subjects).]. 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:11369682; 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:NP318726.RA2OsChAkADnbvb9kkuDP_s4frXPJwtO3p8I8Kt1KImQA130_publicationInfo { this: dcterms:created "2016-05-13T12:44:10+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" . }