@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP297178.RAwXUpCcddM2F8unXOVRDt_UUfKiXOqHayOYKkUo7BZ2E> .
@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:NP297178.RAwXUpCcddM2F8unXOVRDt_UUfKiXOqHayOYKkUo7BZ2E130_head {
  this: np:hasAssertion dgn-np:NP297178.RAwXUpCcddM2F8unXOVRDt_UUfKiXOqHayOYKkUo7BZ2E130_assertion;
    np:hasProvenance dgn-np:NP297178.RAwXUpCcddM2F8unXOVRDt_UUfKiXOqHayOYKkUo7BZ2E130_provenance;
    np:hasPublicationInfo dgn-np:NP297178.RAwXUpCcddM2F8unXOVRDt_UUfKiXOqHayOYKkUo7BZ2E130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP297178.RAwXUpCcddM2F8unXOVRDt_UUfKiXOqHayOYKkUo7BZ2E130_assertion a np:Assertion .
  
  dgn-np:NP297178.RAwXUpCcddM2F8unXOVRDt_UUfKiXOqHayOYKkUo7BZ2E130_provenance a np:Provenance .
  
  dgn-np:NP297178.RAwXUpCcddM2F8unXOVRDt_UUfKiXOqHayOYKkUo7BZ2E130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP297178.RAwXUpCcddM2F8unXOVRDt_UUfKiXOqHayOYKkUo7BZ2E130_assertion {
  miriam-gene:5243 a ncit:C16612 .
  
  lld:C0854467 a ncit:C7057 .
  
  dgn-gda:DGN8998196c6571356432376c61bec884ef sio:SIO_000628 miriam-gene:5243, lld:C0854467;
    a sio:SIO_001121 .
}

dgn-np:NP297178.RAwXUpCcddM2F8unXOVRDt_UUfKiXOqHayOYKkUo7BZ2E130_provenance {
  dgn-np:NP297178.RAwXUpCcddM2F8unXOVRDt_UUfKiXOqHayOYKkUo7BZ2E130_assertion dcterms:description
      "[DNA was extracted from the patients' mononuclear cells and genotyping of O-methylguanine-DNA-methyltransferase (MGMT), multidrug resistance (MDR1; also known as ABCB1), NQO1, and GSTP1 genes and analysis for the epigenetic silencing of specific MGMT gene promoters were carried out to evaluate the possible genetic determinants of increased risk of severe TMZ-induced myelosuppression.]. 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:20938339;
    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:NP297178.RAwXUpCcddM2F8unXOVRDt_UUfKiXOqHayOYKkUo7BZ2E130_publicationInfo {
  this: dcterms:created "2014-10-02T12:34:49+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" .
}