@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP632781.RApVKzx2Rc8FIgVKFHP_3FJ7dN_BbvJYeSH6ImjkkwcWI> .
@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:NP632781.RApVKzx2Rc8FIgVKFHP_3FJ7dN_BbvJYeSH6ImjkkwcWI130_head {
  this: np:hasAssertion dgn-np:NP632781.RApVKzx2Rc8FIgVKFHP_3FJ7dN_BbvJYeSH6ImjkkwcWI130_assertion;
    np:hasProvenance dgn-np:NP632781.RApVKzx2Rc8FIgVKFHP_3FJ7dN_BbvJYeSH6ImjkkwcWI130_provenance;
    np:hasPublicationInfo dgn-np:NP632781.RApVKzx2Rc8FIgVKFHP_3FJ7dN_BbvJYeSH6ImjkkwcWI130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP632781.RApVKzx2Rc8FIgVKFHP_3FJ7dN_BbvJYeSH6ImjkkwcWI130_assertion a np:Assertion .
  
  dgn-np:NP632781.RApVKzx2Rc8FIgVKFHP_3FJ7dN_BbvJYeSH6ImjkkwcWI130_provenance a np:Provenance .
  
  dgn-np:NP632781.RApVKzx2Rc8FIgVKFHP_3FJ7dN_BbvJYeSH6ImjkkwcWI130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP632781.RApVKzx2Rc8FIgVKFHP_3FJ7dN_BbvJYeSH6ImjkkwcWI130_assertion {
  miriam-gene:23038 a ncit:C16612 .
  
  lld:C1704436 a ncit:C7057 .
  
  dgn-gda:DGNbd5597e5140efb8199e99e2244324ff3 sio:SIO_000628 miriam-gene:23038, lld:C1704436;
    a sio:SIO_001121 .
}

dgn-np:NP632781.RApVKzx2Rc8FIgVKFHP_3FJ7dN_BbvJYeSH6ImjkkwcWI130_provenance {
  dgn-np:NP632781.RApVKzx2Rc8FIgVKFHP_3FJ7dN_BbvJYeSH6ImjkkwcWI130_assertion dcterms:description
      "[The aims of this study were to investigate (1) if P2Y(12) polymorphisms defining the P2Y(12) H2 allele are associated with any other SNPs that may explain the previously reported association with increased ADP induced platelet activation and association with peripheral arterial disease and coronary artery disease and (2) if such variants are associated with acute myocardial infarction (AMI) or classical risk factors for AMI.]. 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:18213371;
    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:NP632781.RApVKzx2Rc8FIgVKFHP_3FJ7dN_BbvJYeSH6ImjkkwcWI130_publicationInfo {
  this: dcterms:created "2014-10-02T12:38:22+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" .
}