@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:NP570832.RAl0woXsWsowlyunYvbk1_yVqRn0sr6oKBjzs5rkSwno0130_head { this: np:hasAssertion dgn-np:NP570832.RAl0woXsWsowlyunYvbk1_yVqRn0sr6oKBjzs5rkSwno0130_assertion; np:hasProvenance dgn-np:NP570832.RAl0woXsWsowlyunYvbk1_yVqRn0sr6oKBjzs5rkSwno0130_provenance; np:hasPublicationInfo dgn-np:NP570832.RAl0woXsWsowlyunYvbk1_yVqRn0sr6oKBjzs5rkSwno0130_publicationInfo; a np:Nanopublication . dgn-np:NP570832.RAl0woXsWsowlyunYvbk1_yVqRn0sr6oKBjzs5rkSwno0130_assertion a np:Assertion . dgn-np:NP570832.RAl0woXsWsowlyunYvbk1_yVqRn0sr6oKBjzs5rkSwno0130_provenance a np:Provenance . dgn-np:NP570832.RAl0woXsWsowlyunYvbk1_yVqRn0sr6oKBjzs5rkSwno0130_publicationInfo a np:PublicationInfo . } dgn-np:NP570832.RAl0woXsWsowlyunYvbk1_yVqRn0sr6oKBjzs5rkSwno0130_assertion { miriam-gene:185 a ncit:C16612 . lld:C0027051 a ncit:C7057 . dgn-gda:DGNcd9d69bd5b999b70bca0d080936631ec sio:SIO_000628 miriam-gene:185, lld:C0027051; a sio:SIO_001122 . } dgn-np:NP570832.RAl0woXsWsowlyunYvbk1_yVqRn0sr6oKBjzs5rkSwno0130_provenance { dgn-np:NP570832.RAl0woXsWsowlyunYvbk1_yVqRn0sr6oKBjzs5rkSwno0130_assertion dcterms:description "[Although there have been several association studies of angiotensin II type 1 receptor (AT1R, A/C1166) gene polymorphism in clinical endpoints such as myocardial infarction (MI), hypertension, aortic stiffness, and left ventricular mass, the relationship between AT1R polymorphism and biventricular function in acute anterior MI has not been studied before.]. 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:16998258; 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:NP570832.RAl0woXsWsowlyunYvbk1_yVqRn0sr6oKBjzs5rkSwno0130_publicationInfo { this: dcterms:created "2016-05-13T12:46:03+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" . }