@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP773844.RARu354Vz-N5x4WJSNRCvPktNVmaGNhnQ63L05omrRtSE> .
@prefix rdfs: <http://www.w3.org/2000/01/rdf-schema#> .
@prefix xsd: <http://www.w3.org/2001/XMLSchema#> .
@prefix sio: <http://semanticscience.org/resource/> .
@prefix ncit: <http://ncicb.nci.nih.gov/xml/owl/EVS/Thesaurus.owl#> .
@prefix lld: <http://linkedlifedata.com/resource/umls/id/> .
@prefix miriam-gene: <http://identifiers.org/ncbigene/> .
@prefix miriam-pubmed: <http://identifiers.org/pubmed/> .
@prefix eco: <http://purl.obolibrary.org/obo/eco.owl#> .
@prefix wi: <http://purl.org/ontology/wi/core#> .
@prefix prov: <http://www.w3.org/ns/prov#> .
@prefix pav: <http://purl.org/pav/2.0/> .
@prefix prv: <http://purl.org/net/provenance/ns#> .
@prefix dcterms: <http://purl.org/dc/terms/> .
@prefix np: <http://www.nanopub.org/nschema#> .
@prefix dgn-np: <http://rdf.disgenet.org/nanopublications.trig#> .
@prefix dgn-gda: <http://rdf.disgenet.org/gene-disease-association.ttl#> .
@prefix dgn-void: <http://rdf.disgenet.org/v2.1.0/void.ttl#> .

dgn-np:NP773844.RARu354Vz-N5x4WJSNRCvPktNVmaGNhnQ63L05omrRtSE130_head {
  this: np:hasAssertion dgn-np:NP773844.RARu354Vz-N5x4WJSNRCvPktNVmaGNhnQ63L05omrRtSE130_assertion;
    np:hasProvenance dgn-np:NP773844.RARu354Vz-N5x4WJSNRCvPktNVmaGNhnQ63L05omrRtSE130_provenance;
    np:hasPublicationInfo dgn-np:NP773844.RARu354Vz-N5x4WJSNRCvPktNVmaGNhnQ63L05omrRtSE130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP773844.RARu354Vz-N5x4WJSNRCvPktNVmaGNhnQ63L05omrRtSE130_assertion a np:Assertion .
  
  dgn-np:NP773844.RARu354Vz-N5x4WJSNRCvPktNVmaGNhnQ63L05omrRtSE130_provenance a np:Provenance .
  
  dgn-np:NP773844.RARu354Vz-N5x4WJSNRCvPktNVmaGNhnQ63L05omrRtSE130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP773844.RARu354Vz-N5x4WJSNRCvPktNVmaGNhnQ63L05omrRtSE130_assertion {
  miriam-gene:4846 a ncit:C16612 .
  
  lld:C0340557 a ncit:C7057 .
  
  dgn-gda:DGNa1304719ef981ddf5b777e292182cb3d sio:SIO_000628 miriam-gene:4846, lld:C0340557;
    a sio:SIO_001121 .
}

dgn-np:NP773844.RARu354Vz-N5x4WJSNRCvPktNVmaGNhnQ63L05omrRtSE130_provenance {
  dgn-np:NP773844.RARu354Vz-N5x4WJSNRCvPktNVmaGNhnQ63L05omrRtSE130_assertion dcterms:description
      "[The Asp allele of the eNOS Glu298Asp polymorphism was associated with atherosclerotic renal artery stenosis with an odds ratio of 1.44 (95% confidence interval 1.00 to 2.09) versus hypertensives with angiographically proven patent arteries, of 1.89 (1.24 to 2.87) versus hypertensive family practice controls, and of 2.09 (1.29 to 3.38) versus normotensive family practice controls.]. 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:15326089;
    prov:wasDerivedFrom dgn-void:befree-20140225;
    prov:wasGeneratedBy eco:ECO_0000203 .
  
  dgn-void:befree-20140225 pav:importedOn "2014-02-25"^^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:NP773844.RARu354Vz-N5x4WJSNRCvPktNVmaGNhnQ63L05omrRtSE130_publicationInfo {
  this: dcterms:created "2014-10-02T12:39:48+02:00"^^xsd:dateTime;
    dcterms:rights <http://opendatacommons.org/licenses/odbl/1.0/>;
    dcterms:rightsHolder dgn-void:IBIGroup;
    dcterms:subject sio:SIO_000983;
    prv:usedData dgn-void:disgenetrdf;
    pav:authoredBy <http://orcid.org/0000-0001-5999-6269>, <http://orcid.org/0000-0002-7534-7661>,
      <http://orcid.org/0000-0002-9383-528X>, <http://orcid.org/0000-0003-0169-8159>, <http://orcid.org/0000-0003-1244-7654>;
    pav:createdBy <http://orcid.org/0000-0003-0169-8159>;
    pav:version "v2.1.0.0" .
  
  dgn-void:disgenetrdf pav:version "v2.1.0" .
}