@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:NP870889.RA5Y9QJM9k15dpme65qgt5TJftWST3R5NFLR3lParDKFQ130_head { this: np:hasAssertion dgn-np:NP870889.RA5Y9QJM9k15dpme65qgt5TJftWST3R5NFLR3lParDKFQ130_assertion; np:hasProvenance dgn-np:NP870889.RA5Y9QJM9k15dpme65qgt5TJftWST3R5NFLR3lParDKFQ130_provenance; np:hasPublicationInfo dgn-np:NP870889.RA5Y9QJM9k15dpme65qgt5TJftWST3R5NFLR3lParDKFQ130_publicationInfo; a np:Nanopublication . dgn-np:NP870889.RA5Y9QJM9k15dpme65qgt5TJftWST3R5NFLR3lParDKFQ130_assertion a np:Assertion . dgn-np:NP870889.RA5Y9QJM9k15dpme65qgt5TJftWST3R5NFLR3lParDKFQ130_provenance a np:Provenance . dgn-np:NP870889.RA5Y9QJM9k15dpme65qgt5TJftWST3R5NFLR3lParDKFQ130_publicationInfo a np:PublicationInfo . } dgn-np:NP870889.RA5Y9QJM9k15dpme65qgt5TJftWST3R5NFLR3lParDKFQ130_assertion { miriam-gene:23327 a ncit:C16612 . lld:C0038454 a ncit:C7057 . dgn-gda:DGN75da11a8e16e1ac33519763af15ef12d sio:SIO_000628 miriam-gene:23327, lld:C0038454; a sio:SIO_001121 . } dgn-np:NP870889.RA5Y9QJM9k15dpme65qgt5TJftWST3R5NFLR3lParDKFQ130_provenance { dgn-np:NP870889.RA5Y9QJM9k15dpme65qgt5TJftWST3R5NFLR3lParDKFQ130_assertion dcterms:description "[Carriers of the NEDD4L salt sensitivity-associated genotype had (mean ± SEM) higher systolic (142 ± 0.4 vs. 141 ± 0.1 mmHg, P = 0.002) and diastolic (86.0 ± 0.5 vs. 85.6 ± 0.2 mmHg, P = 0.025) blood pressure and multivariate adjusted hazards ratio (95% confidence interval) of CVD 1.13 (1.02-1.25, P = 0.018), coronary events 1.20 (1.06-1.37; P = 0.005) and cardiovascular mortality 1.17 (0.99-1.37; P = 0.055) than noncarriers but there was no significant difference in the incidence of stroke and total mortality.]. 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:24284497; prov:wasDerivedFrom dgn-void:befree-20150227; prov:wasGeneratedBy eco:ECO_0000203 . dgn-void:befree-20150227 pav:importedOn "2015-02-27"^^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:NP870889.RA5Y9QJM9k15dpme65qgt5TJftWST3R5NFLR3lParDKFQ130_publicationInfo { this: dcterms:created "2015-08-25T14:46:29+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 "v3.0.0.0" . dgn-void:disgenetv3.0rdf pav:version "v3.0.0" . }