@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP539552.RAKJ37LQwl2rTvu06X0aS3EXpNXqne2rIMn5HUnD2fGwk> .
@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:NP539552.RAKJ37LQwl2rTvu06X0aS3EXpNXqne2rIMn5HUnD2fGwk130_head {
  this: np:hasAssertion dgn-np:NP539552.RAKJ37LQwl2rTvu06X0aS3EXpNXqne2rIMn5HUnD2fGwk130_assertion ;
    np:hasProvenance dgn-np:NP539552.RAKJ37LQwl2rTvu06X0aS3EXpNXqne2rIMn5HUnD2fGwk130_provenance ;
    np:hasPublicationInfo dgn-np:NP539552.RAKJ37LQwl2rTvu06X0aS3EXpNXqne2rIMn5HUnD2fGwk130_publicationInfo ;
    a np:Nanopublication .
  dgn-np:NP539552.RAKJ37LQwl2rTvu06X0aS3EXpNXqne2rIMn5HUnD2fGwk130_assertion a np:Assertion .
  dgn-np:NP539552.RAKJ37LQwl2rTvu06X0aS3EXpNXqne2rIMn5HUnD2fGwk130_provenance a np:Provenance .
  dgn-np:NP539552.RAKJ37LQwl2rTvu06X0aS3EXpNXqne2rIMn5HUnD2fGwk130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP539552.RAKJ37LQwl2rTvu06X0aS3EXpNXqne2rIMn5HUnD2fGwk130_assertion {
  miriam-gene:1465 a ncit:C16612 .
  lld:C0155626 a ncit:C7057 .
  dgn-gda:DGN41d8f2d97886acbf9b584b5340852263 sio:SIO_000628 miriam-gene:1465 , lld:C0155626 ;
    a sio:SIO_001121 .
}
dgn-np:NP539552.RAKJ37LQwl2rTvu06X0aS3EXpNXqne2rIMn5HUnD2fGwk130_provenance {
  dgn-np:NP539552.RAKJ37LQwl2rTvu06X0aS3EXpNXqne2rIMn5HUnD2fGwk130_assertion dcterms:description "[We collected conventional (blood pressure, cholesterol, adiposity), lifestyle, and novel (C-reactive protein, CRP) risk factors at baseline in participants from the Scottish Health Surveys (n = 5946, 44.5% men, aged 53.6 +/- 12.4 years), who were followed up over an average of 7.1 years for cardiovascular disease (CVD) events (a composite of fatal and nonfatal events incorporating acute myocardial infarction, coronary artery bypass surgery, percutaneous coronary angioplasty, stroke, heart failure).]. 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:19587606 ;
    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:NP539552.RAKJ37LQwl2rTvu06X0aS3EXpNXqne2rIMn5HUnD2fGwk130_publicationInfo {
  this: dcterms:created "2014-10-02T12:37:25+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> ;
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}