@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:NP1389854.RA9NoRQQf2BGHsF9L9jR4cNsUth7km17C4IYrH10IgZR4130_head { this: np:hasAssertion dgn-np:NP1389854.RA9NoRQQf2BGHsF9L9jR4cNsUth7km17C4IYrH10IgZR4130_assertion; np:hasProvenance dgn-np:NP1389854.RA9NoRQQf2BGHsF9L9jR4cNsUth7km17C4IYrH10IgZR4130_provenance; np:hasPublicationInfo dgn-np:NP1389854.RA9NoRQQf2BGHsF9L9jR4cNsUth7km17C4IYrH10IgZR4130_publicationInfo; a np:Nanopublication . dgn-np:NP1389854.RA9NoRQQf2BGHsF9L9jR4cNsUth7km17C4IYrH10IgZR4130_assertion a np:Assertion . dgn-np:NP1389854.RA9NoRQQf2BGHsF9L9jR4cNsUth7km17C4IYrH10IgZR4130_provenance a np:Provenance . dgn-np:NP1389854.RA9NoRQQf2BGHsF9L9jR4cNsUth7km17C4IYrH10IgZR4130_publicationInfo a np:PublicationInfo . } dgn-np:NP1389854.RA9NoRQQf2BGHsF9L9jR4cNsUth7km17C4IYrH10IgZR4130_assertion { miriam-gene:4023 a ncit:C16612 . lld:C1956346 a ncit:C7057 . dgn-gda:DGNdf2c913df597eab30da99e708e2aedf5 sio:SIO_000628 miriam-gene:4023, lld:C1956346; a sio:SIO_001121 . } dgn-np:NP1389854.RA9NoRQQf2BGHsF9L9jR4cNsUth7km17C4IYrH10IgZR4130_provenance { dgn-np:NP1389854.RA9NoRQQf2BGHsF9L9jR4cNsUth7km17C4IYrH10IgZR4130_assertion dcterms:description "[The association of genetic markers at the apolipoprotein B gene (APOB) (XbaI, MspI, and EcoRI polymorphisms) and the lipoprotein lipase gene (LPL) (PvuII polymorphism) with coronary artery disease (CAD) and with variation in plasma lipid levels (total cholesterol, high-density lipoprotein cholesterol, and total triglycerides) was studied in 94 male patients with CAD diagnosed by angiography and in 122 unrelated men of Russian descent free of clinical signs of CAD.]. 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:9489234; 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:NP1389854.RA9NoRQQf2BGHsF9L9jR4cNsUth7km17C4IYrH10IgZR4130_publicationInfo { this: dcterms:created "2016-05-13T12:52:16+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" . }