@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP524756.RA6V2g1VT1FgOlfNuBqATAaz9t_106P0teN1XJi2eyPbk> .
@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:NP524756.RA6V2g1VT1FgOlfNuBqATAaz9t_106P0teN1XJi2eyPbk130_head {
  this: np:hasAssertion dgn-np:NP524756.RA6V2g1VT1FgOlfNuBqATAaz9t_106P0teN1XJi2eyPbk130_assertion;
    np:hasProvenance dgn-np:NP524756.RA6V2g1VT1FgOlfNuBqATAaz9t_106P0teN1XJi2eyPbk130_provenance;
    np:hasPublicationInfo dgn-np:NP524756.RA6V2g1VT1FgOlfNuBqATAaz9t_106P0teN1XJi2eyPbk130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP524756.RA6V2g1VT1FgOlfNuBqATAaz9t_106P0teN1XJi2eyPbk130_assertion a np:Assertion .
  
  dgn-np:NP524756.RA6V2g1VT1FgOlfNuBqATAaz9t_106P0teN1XJi2eyPbk130_provenance a np:Provenance .
  
  dgn-np:NP524756.RA6V2g1VT1FgOlfNuBqATAaz9t_106P0teN1XJi2eyPbk130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP524756.RA6V2g1VT1FgOlfNuBqATAaz9t_106P0teN1XJi2eyPbk130_assertion {
  miriam-gene:1557 a ncit:C16612 .
  
  lld:C0038454 a ncit:C7057 .
  
  dgn-gda:DGN005883a2fe3db7e57d7432984724f9f9 sio:SIO_000628 miriam-gene:1557, lld:C0038454;
    a sio:SIO_001121 .
}

dgn-np:NP524756.RA6V2g1VT1FgOlfNuBqATAaz9t_106P0teN1XJi2eyPbk130_provenance {
  dgn-np:NP524756.RA6V2g1VT1FgOlfNuBqATAaz9t_106P0teN1XJi2eyPbk130_assertion dcterms:description
      "[We then assessed the relation of allelic variants of genes modulating clopidogrel absorption (ABCB1), metabolic activation (CYP3A5 and CYP2C19), and biologic activity (P2RY12 and ITGB3) to the risk of death from any cause, nonfatal stroke, or myocardial infarction during 1 year of follow-up.]. 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:19106083;
    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:NP524756.RA6V2g1VT1FgOlfNuBqATAaz9t_106P0teN1XJi2eyPbk130_publicationInfo {
  this: dcterms:created "2014-10-02T12:37:15+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" .
}