@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP490662.RAxuypPQPd4O6qj5UklSo93dAbd9ALv52Lic1WbdAIepc> .
@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:NP490662.RAxuypPQPd4O6qj5UklSo93dAbd9ALv52Lic1WbdAIepc130_head {
  this: np:hasAssertion dgn-np:NP490662.RAxuypPQPd4O6qj5UklSo93dAbd9ALv52Lic1WbdAIepc130_assertion ;
    np:hasProvenance dgn-np:NP490662.RAxuypPQPd4O6qj5UklSo93dAbd9ALv52Lic1WbdAIepc130_provenance ;
    np:hasPublicationInfo dgn-np:NP490662.RAxuypPQPd4O6qj5UklSo93dAbd9ALv52Lic1WbdAIepc130_publicationInfo ;
    a np:Nanopublication .
  dgn-np:NP490662.RAxuypPQPd4O6qj5UklSo93dAbd9ALv52Lic1WbdAIepc130_assertion a np:Assertion .
  dgn-np:NP490662.RAxuypPQPd4O6qj5UklSo93dAbd9ALv52Lic1WbdAIepc130_provenance a np:Provenance .
  dgn-np:NP490662.RAxuypPQPd4O6qj5UklSo93dAbd9ALv52Lic1WbdAIepc130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP490662.RAxuypPQPd4O6qj5UklSo93dAbd9ALv52Lic1WbdAIepc130_assertion {
  miriam-gene:1917 a ncit:C16612 .
  lld:C0027051 a ncit:C7057 .
  dgn-gda:DGN9320909123547d5ae50288cb1c776238 sio:SIO_000628 miriam-gene:1917 , lld:C0027051 ;
    a sio:SIO_001121 .
}
dgn-np:NP490662.RAxuypPQPd4O6qj5UklSo93dAbd9ALv52Lic1WbdAIepc130_provenance {
  dgn-np:NP490662.RAxuypPQPd4O6qj5UklSo93dAbd9ALv52Lic1WbdAIepc130_assertion dcterms:description "[We genotyped 1,778 acute coronary syndrome patients within the PROVE IT-TIMI 22 (Pravastatin or Atorvastatin Evaluation and Infection Therapy: Thrombolysis in Myocardial Infarction 22) trial and investigated different intensities of statin therapy in carriers of 719Arg and in noncarriers using Cox proportional hazards models that adjusted for traditional risk factors.]. 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:18222355 ;
    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:NP490662.RAxuypPQPd4O6qj5UklSo93dAbd9ALv52Lic1WbdAIepc130_publicationInfo {
  this: dcterms:created "2014-10-02T12:36:53+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" .
}