@prefix this: <http://rdf.disgenet.org/resource/nanopub/NP66911.RAffn_UklziISYunW9Lmpsf5izVcSvHnEanM3ahTaCsOo> .
@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/> .
@prefix wi: <http://purl.org/ontology/wi/core#> .
@prefix prov: <http://www.w3.org/ns/prov#> .
@prefix pav: <http://purl.org/pav/> .
@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/resource/nanopub/> .
@prefix dgn-gda: <http://rdf.disgenet.org/resource/gda/> .
@prefix dgn-void: <http://rdf.disgenet.org/v3.0.0/void/> .

dgn-np:NP66911.RAffn_UklziISYunW9Lmpsf5izVcSvHnEanM3ahTaCsOo130_head {
  this: np:hasAssertion dgn-np:NP66911.RAffn_UklziISYunW9Lmpsf5izVcSvHnEanM3ahTaCsOo130_assertion;
    np:hasProvenance dgn-np:NP66911.RAffn_UklziISYunW9Lmpsf5izVcSvHnEanM3ahTaCsOo130_provenance;
    np:hasPublicationInfo dgn-np:NP66911.RAffn_UklziISYunW9Lmpsf5izVcSvHnEanM3ahTaCsOo130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP66911.RAffn_UklziISYunW9Lmpsf5izVcSvHnEanM3ahTaCsOo130_assertion a np:Assertion .
  
  dgn-np:NP66911.RAffn_UklziISYunW9Lmpsf5izVcSvHnEanM3ahTaCsOo130_provenance a np:Provenance .
  
  dgn-np:NP66911.RAffn_UklziISYunW9Lmpsf5izVcSvHnEanM3ahTaCsOo130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP66911.RAffn_UklziISYunW9Lmpsf5izVcSvHnEanM3ahTaCsOo130_assertion {
  miriam-gene:64805 a ncit:C16612 .
  
  lld:C0085096 a ncit:C7057 .
  
  dgn-gda:DGN9ac541b8bf1fe03e5f21cb0a4fc23a93 sio:SIO_000628 miriam-gene:64805, lld:C0085096;
    a sio:SIO_001122 .
}

dgn-np:NP66911.RAffn_UklziISYunW9Lmpsf5izVcSvHnEanM3ahTaCsOo130_provenance {
  dgn-np:NP66911.RAffn_UklziISYunW9Lmpsf5izVcSvHnEanM3ahTaCsOo130_assertion dcterms:description
      "[ In PAD patients, clopidogrel response variability exists, which may result in increased risk for cerebrovascular events. Sequence alterations of the target receptor gene represent one possible mechanism for clopidogrel failure. Whether identification of ]. 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:15933261;
    prov:wasDerivedFrom dgn-void:gad-20150221;
    prov:wasGeneratedBy eco:ECO_0000203 .
  
  dgn-void:gad-20150221 pav:importedOn "2015-02-21"^^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:NP66911.RAffn_UklziISYunW9Lmpsf5izVcSvHnEanM3ahTaCsOo130_publicationInfo {
  this: dcterms:created "2015-08-25T14:38:16+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:disgenetv3.0rdf;
    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 "v3.0.0.0" .
  
  dgn-void:disgenetv3.0rdf pav:version "v3.0.0" .
}