@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP556113.RAjBZEioAIUCh7PIKT5JyH16uhJbr2q4bEkoifKDO93YI> .
@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:NP556113.RAjBZEioAIUCh7PIKT5JyH16uhJbr2q4bEkoifKDO93YI130_head {
  this: np:hasAssertion dgn-np:NP556113.RAjBZEioAIUCh7PIKT5JyH16uhJbr2q4bEkoifKDO93YI130_assertion ;
    np:hasProvenance dgn-np:NP556113.RAjBZEioAIUCh7PIKT5JyH16uhJbr2q4bEkoifKDO93YI130_provenance ;
    np:hasPublicationInfo dgn-np:NP556113.RAjBZEioAIUCh7PIKT5JyH16uhJbr2q4bEkoifKDO93YI130_publicationInfo ;
    a np:Nanopublication .
  dgn-np:NP556113.RAjBZEioAIUCh7PIKT5JyH16uhJbr2q4bEkoifKDO93YI130_assertion a np:Assertion .
  dgn-np:NP556113.RAjBZEioAIUCh7PIKT5JyH16uhJbr2q4bEkoifKDO93YI130_provenance a np:Provenance .
  dgn-np:NP556113.RAjBZEioAIUCh7PIKT5JyH16uhJbr2q4bEkoifKDO93YI130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP556113.RAjBZEioAIUCh7PIKT5JyH16uhJbr2q4bEkoifKDO93YI130_assertion {
  miriam-gene:1557 a ncit:C16612 .
  lld:C1956346 a ncit:C7057 .
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    a sio:SIO_001121 .
}
dgn-np:NP556113.RAjBZEioAIUCh7PIKT5JyH16uhJbr2q4bEkoifKDO93YI130_provenance {
  dgn-np:NP556113.RAjBZEioAIUCh7PIKT5JyH16uhJbr2q4bEkoifKDO93YI130_assertion dcterms:description "[Loss-of-function (LOF) variants of cytochrome P450 2C19 (CYP2C19) have been hypothesized to be associated with lesser degrees of platelet inhibition and increased risk for recurrent ischemic events in patients with coronary artery disease on clopidogrel therapy; however, studies from Western countries have yielded mixed results.]. 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:22591668 ;
    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:NP556113.RAjBZEioAIUCh7PIKT5JyH16uhJbr2q4bEkoifKDO93YI130_publicationInfo {
  this: dcterms:created "2014-10-02T12:37:35+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 ;
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}