@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:NP898515.RAD_IMLWNvNSw0UGyM55nBfd0tG9Zi27hdNhUOxxf2fpA130_head { this: np:hasAssertion dgn-np:NP898515.RAD_IMLWNvNSw0UGyM55nBfd0tG9Zi27hdNhUOxxf2fpA130_assertion; np:hasProvenance dgn-np:NP898515.RAD_IMLWNvNSw0UGyM55nBfd0tG9Zi27hdNhUOxxf2fpA130_provenance; np:hasPublicationInfo dgn-np:NP898515.RAD_IMLWNvNSw0UGyM55nBfd0tG9Zi27hdNhUOxxf2fpA130_publicationInfo; a np:Nanopublication . dgn-np:NP898515.RAD_IMLWNvNSw0UGyM55nBfd0tG9Zi27hdNhUOxxf2fpA130_assertion a np:Assertion . dgn-np:NP898515.RAD_IMLWNvNSw0UGyM55nBfd0tG9Zi27hdNhUOxxf2fpA130_provenance a np:Provenance . dgn-np:NP898515.RAD_IMLWNvNSw0UGyM55nBfd0tG9Zi27hdNhUOxxf2fpA130_publicationInfo a np:PublicationInfo . } dgn-np:NP898515.RAD_IMLWNvNSw0UGyM55nBfd0tG9Zi27hdNhUOxxf2fpA130_assertion { miriam-gene:4846 a ncit:C16612 . lld:C0162869 a ncit:C7057 . dgn-gda:DGN2d798f3d0f25d4724f5b855095ecf7a9 sio:SIO_000628 miriam-gene:4846, lld:C0162869; a sio:SIO_001122 . } dgn-np:NP898515.RAD_IMLWNvNSw0UGyM55nBfd0tG9Zi27hdNhUOxxf2fpA130_provenance { dgn-np:NP898515.RAD_IMLWNvNSw0UGyM55nBfd0tG9Zi27hdNhUOxxf2fpA130_assertion dcterms:description "[Three eNOS polymorphisms (eNOS 27VNTR, T786C, and G894T) were genotyped in 96 patients with ruptured aneurysms, 53 patients with unruptured aneurysms, and in 121 volunteers via polymerase chain reaction-restriction fragment length polymorphism analysis.]. 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:21631225; 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:NP898515.RAD_IMLWNvNSw0UGyM55nBfd0tG9Zi27hdNhUOxxf2fpA130_publicationInfo { this: dcterms:created "2016-05-13T12:48:31+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" . }