@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP54746.RAkgN13MgOAcNmLcoeZtLSpTiwtzJOZWw1oTfahaqpDlc> .
@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#> .
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  this: np:hasAssertion dgn-np:NP54746.RAkgN13MgOAcNmLcoeZtLSpTiwtzJOZWw1oTfahaqpDlc130_assertion ;
    np:hasProvenance dgn-np:NP54746.RAkgN13MgOAcNmLcoeZtLSpTiwtzJOZWw1oTfahaqpDlc130_provenance ;
    np:hasPublicationInfo dgn-np:NP54746.RAkgN13MgOAcNmLcoeZtLSpTiwtzJOZWw1oTfahaqpDlc130_publicationInfo ;
    a np:Nanopublication .
  dgn-np:NP54746.RAkgN13MgOAcNmLcoeZtLSpTiwtzJOZWw1oTfahaqpDlc130_assertion a np:Assertion .
  dgn-np:NP54746.RAkgN13MgOAcNmLcoeZtLSpTiwtzJOZWw1oTfahaqpDlc130_provenance a np:Provenance .
  dgn-np:NP54746.RAkgN13MgOAcNmLcoeZtLSpTiwtzJOZWw1oTfahaqpDlc130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP54746.RAkgN13MgOAcNmLcoeZtLSpTiwtzJOZWw1oTfahaqpDlc130_assertion {
  miriam-gene:4255 a ncit:C16612 .
  lld:C0153633 a ncit:C7057 .
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dgn-np:NP54746.RAkgN13MgOAcNmLcoeZtLSpTiwtzJOZWw1oTfahaqpDlc130_provenance {
  dgn-np:NP54746.RAkgN13MgOAcNmLcoeZtLSpTiwtzJOZWw1oTfahaqpDlc130_assertion dcterms:description "[ Our results are consistent with ethnic variation in glioma pathogenesis. The data on MGMT show that an inherited factor involving the repair of methylation and other alkylation damage, specifically to the O6 position of guanine, may be associated with the development of tumors that proceed in their development without TP53 mutations or accumulation of TP53 protein and possibly also those that do not involve amplification of the EGFR locus.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ;
    wi:evidence dgn-void:source_evidence_literature ;
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    prov:wasDerivedFrom dgn-void:gad-20130706 ;
    prov:wasGeneratedBy eco:ECO_0000203 .
  dgn-void:gad-20130706 pav:importedOn "2013-07-06"^^xsd:date .
  dgn-void:source_evidence_literature a eco:ECO_0000212 ;
    rdfs:comment "Gene-disease associations inferred from text-mining the literature."@en ;
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}
dgn-np:NP54746.RAkgN13MgOAcNmLcoeZtLSpTiwtzJOZWw1oTfahaqpDlc130_publicationInfo {
  this: dcterms:created "2014-10-02T12:32:25+02:00"^^xsd:dateTime ;
    dcterms:rights <http://opendatacommons.org/licenses/odbl/1.0/> ;
    dcterms:rightsHolder dgn-void:IBIGroup ;
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}