@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP659426.RAj-yFw15FerC68Z_89iz4nK08_MyHN2R0h2Dq7AcZgUA> .
@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:NP659426.RAj-yFw15FerC68Z_89iz4nK08_MyHN2R0h2Dq7AcZgUA130_head {
  this: np:hasAssertion dgn-np:NP659426.RAj-yFw15FerC68Z_89iz4nK08_MyHN2R0h2Dq7AcZgUA130_assertion;
    np:hasProvenance dgn-np:NP659426.RAj-yFw15FerC68Z_89iz4nK08_MyHN2R0h2Dq7AcZgUA130_provenance;
    np:hasPublicationInfo dgn-np:NP659426.RAj-yFw15FerC68Z_89iz4nK08_MyHN2R0h2Dq7AcZgUA130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP659426.RAj-yFw15FerC68Z_89iz4nK08_MyHN2R0h2Dq7AcZgUA130_assertion a np:Assertion .
  
  dgn-np:NP659426.RAj-yFw15FerC68Z_89iz4nK08_MyHN2R0h2Dq7AcZgUA130_provenance a np:Provenance .
  
  dgn-np:NP659426.RAj-yFw15FerC68Z_89iz4nK08_MyHN2R0h2Dq7AcZgUA130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP659426.RAj-yFw15FerC68Z_89iz4nK08_MyHN2R0h2Dq7AcZgUA130_assertion {
  miriam-gene:1244 a ncit:C16612 .
  
  lld:C0014544 a ncit:C7057 .
  
  dgn-gda:DGN9bb72ef907e14cb60b8d0628dde0163c sio:SIO_000628 miriam-gene:1244, lld:C0014544;
    a sio:SIO_001121 .
}

dgn-np:NP659426.RAj-yFw15FerC68Z_89iz4nK08_MyHN2R0h2Dq7AcZgUA130_provenance {
  dgn-np:NP659426.RAj-yFw15FerC68Z_89iz4nK08_MyHN2R0h2Dq7AcZgUA130_assertion dcterms:description
      "[We aimed to evaluate the association of non-response to antiepileptic pharmacotherapy with the frequency of variant alleles in the drug transporter genes ABCB1 and ABCC2 or in the CYP2C locus in young patients with epilepsy and an independent cohort of adults with drug-refractory epilepsy.]. 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:19415824;
    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:NP659426.RAj-yFw15FerC68Z_89iz4nK08_MyHN2R0h2Dq7AcZgUA130_publicationInfo {
  this: dcterms:created "2014-10-02T12:38:38+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" .
}