@prefix this: <http://rdf.disgenet.org/resource/nanopub/NP754648.RACqPl1zDHiW7uaKeAoQaMs7kvTZdXjzt_SBp5PfnGEe8> .
@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/> .
@prefix wi: <http://purl.org/ontology/wi/core#> .
@prefix prov: <http://www.w3.org/ns/prov#> .
@prefix pav: <http://purl.org/pav/> .
@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/resource/nanopub/> .
@prefix dgn-gda: <http://rdf.disgenet.org/resource/gda/> .
@prefix dgn-void: <http://rdf.disgenet.org/v3.0.0/void/> .

dgn-np:NP754648.RACqPl1zDHiW7uaKeAoQaMs7kvTZdXjzt_SBp5PfnGEe8130_head {
  this: np:hasAssertion dgn-np:NP754648.RACqPl1zDHiW7uaKeAoQaMs7kvTZdXjzt_SBp5PfnGEe8130_assertion;
    np:hasProvenance dgn-np:NP754648.RACqPl1zDHiW7uaKeAoQaMs7kvTZdXjzt_SBp5PfnGEe8130_provenance;
    np:hasPublicationInfo dgn-np:NP754648.RACqPl1zDHiW7uaKeAoQaMs7kvTZdXjzt_SBp5PfnGEe8130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP754648.RACqPl1zDHiW7uaKeAoQaMs7kvTZdXjzt_SBp5PfnGEe8130_assertion a np:Assertion .
  
  dgn-np:NP754648.RACqPl1zDHiW7uaKeAoQaMs7kvTZdXjzt_SBp5PfnGEe8130_provenance a np:Provenance .
  
  dgn-np:NP754648.RACqPl1zDHiW7uaKeAoQaMs7kvTZdXjzt_SBp5PfnGEe8130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP754648.RACqPl1zDHiW7uaKeAoQaMs7kvTZdXjzt_SBp5PfnGEe8130_assertion {
  miriam-gene:7157 a ncit:C16612 .
  
  lld:C1621958 a ncit:C7057 .
  
  dgn-gda:DGN5f1c1eb3b4c1fb20e9ac05820079105e sio:SIO_000628 miriam-gene:7157, lld:C1621958;
    a sio:SIO_001121 .
}

dgn-np:NP754648.RACqPl1zDHiW7uaKeAoQaMs7kvTZdXjzt_SBp5PfnGEe8130_provenance {
  dgn-np:NP754648.RACqPl1zDHiW7uaKeAoQaMs7kvTZdXjzt_SBp5PfnGEe8130_assertion dcterms:description
      "[To address these issues, we have investigated the MGMT methylation status, clinical and magnetic resonance imaging characteristics, and relevant genetic features (loss of heterozygosity on 17p and 19q, EGFR amplification, and p53 mutations) in a retrospective study on 86 patients affected by glioblastoma multiforme: 72 patients had a clinical history indicating de novo insurgence of the tumor and the remaining 14 were secondary glioblastoma multiforme.]. 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:17473190;
    prov:wasDerivedFrom dgn-void:befree-20150227;
    prov:wasGeneratedBy eco:ECO_0000203 .
  
  dgn-void:befree-20150227 pav:importedOn "2015-02-27"^^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:NP754648.RACqPl1zDHiW7uaKeAoQaMs7kvTZdXjzt_SBp5PfnGEe8130_publicationInfo {
  this: dcterms:created "2015-08-25T14:45:15+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:disgenetv3.0rdf;
    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 "v3.0.0.0" .
  
  dgn-void:disgenetv3.0rdf pav:version "v3.0.0" .
}