@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP367485.RAiMHKMvTlBwwECMzjET92Xnf-tjyxeNkNq-cOi03kADY> .
@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:NP367485.RAiMHKMvTlBwwECMzjET92Xnf-tjyxeNkNq-cOi03kADY130_head {
  this: np:hasAssertion dgn-np:NP367485.RAiMHKMvTlBwwECMzjET92Xnf-tjyxeNkNq-cOi03kADY130_assertion;
    np:hasProvenance dgn-np:NP367485.RAiMHKMvTlBwwECMzjET92Xnf-tjyxeNkNq-cOi03kADY130_provenance;
    np:hasPublicationInfo dgn-np:NP367485.RAiMHKMvTlBwwECMzjET92Xnf-tjyxeNkNq-cOi03kADY130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP367485.RAiMHKMvTlBwwECMzjET92Xnf-tjyxeNkNq-cOi03kADY130_assertion a np:Assertion .
  
  dgn-np:NP367485.RAiMHKMvTlBwwECMzjET92Xnf-tjyxeNkNq-cOi03kADY130_provenance a np:Provenance .
  
  dgn-np:NP367485.RAiMHKMvTlBwwECMzjET92Xnf-tjyxeNkNq-cOi03kADY130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP367485.RAiMHKMvTlBwwECMzjET92Xnf-tjyxeNkNq-cOi03kADY130_assertion {
  miriam-gene:1576 a ncit:C16612 .
  
  lld:C0948089 a ncit:C7057 .
  
  dgn-gda:DGN728a70288b357dc134ba171b3bd03c9f sio:SIO_000628 miriam-gene:1576, lld:C0948089;
    a sio:SIO_001121 .
}

dgn-np:NP367485.RAiMHKMvTlBwwECMzjET92Xnf-tjyxeNkNq-cOi03kADY130_provenance {
  dgn-np:NP367485.RAiMHKMvTlBwwECMzjET92Xnf-tjyxeNkNq-cOi03kADY130_assertion dcterms:description
      "[This research evaluated the frequency of variant alleles in the genes coding for CYP3A4, CYP3A5, CYP2C9, and CYP2C19 enzymes in patients on clopidogrel therapy and experiencing repeat acute coronary syndrome (ACS) compared to a control group with a matching ethnic composition.]. 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:19337788;
    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:NP367485.RAiMHKMvTlBwwECMzjET92Xnf-tjyxeNkNq-cOi03kADY130_publicationInfo {
  this: dcterms:created "2014-10-02T12:35:35+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;
    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" .
}