@prefix this: <http://rdf.disgenet.org/resource/nanopub/NP646113.RAjbx2Wrw40UMZDS8_FST_8oTxNkTS9fQxTQZOqdwn53I> .
@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/v4.0.0/void/> .

dgn-np:NP646113.RAjbx2Wrw40UMZDS8_FST_8oTxNkTS9fQxTQZOqdwn53I130_head {
  this: np:hasAssertion dgn-np:NP646113.RAjbx2Wrw40UMZDS8_FST_8oTxNkTS9fQxTQZOqdwn53I130_assertion;
    np:hasProvenance dgn-np:NP646113.RAjbx2Wrw40UMZDS8_FST_8oTxNkTS9fQxTQZOqdwn53I130_provenance;
    np:hasPublicationInfo dgn-np:NP646113.RAjbx2Wrw40UMZDS8_FST_8oTxNkTS9fQxTQZOqdwn53I130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP646113.RAjbx2Wrw40UMZDS8_FST_8oTxNkTS9fQxTQZOqdwn53I130_assertion a np:Assertion .
  
  dgn-np:NP646113.RAjbx2Wrw40UMZDS8_FST_8oTxNkTS9fQxTQZOqdwn53I130_provenance a np:Provenance .
  
  dgn-np:NP646113.RAjbx2Wrw40UMZDS8_FST_8oTxNkTS9fQxTQZOqdwn53I130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP646113.RAjbx2Wrw40UMZDS8_FST_8oTxNkTS9fQxTQZOqdwn53I130_assertion {
  miriam-gene:4255 a ncit:C16612 .
  
  lld:C0017636 a ncit:C7057 .
  
  dgn-gda:DGN9055aa8a32f986ff742318c2f5123622 sio:SIO_000628 miriam-gene:4255, lld:C0017636;
    a sio:SIO_001121 .
}

dgn-np:NP646113.RAjbx2Wrw40UMZDS8_FST_8oTxNkTS9fQxTQZOqdwn53I130_provenance {
  dgn-np:NP646113.RAjbx2Wrw40UMZDS8_FST_8oTxNkTS9fQxTQZOqdwn53I130_assertion dcterms:description
      "[In particular, the presence or absence of combined 1p/19 loss in oligodendroglial tumors, epidermal growth factor receptor amplification, epidermal growth factor receptor vIII mutations in grade III tumors and glioblastoma multiforme, and MGMT promoter gene methylation in glioblastoma multiforme are now being used to tailor treatment decisions in patients.]. 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:18090916;
    prov:wasDerivedFrom dgn-void:befree-2016;
    prov:wasGeneratedBy eco:ECO_0000203 .
  
  dgn-void:befree-2016 pav:importedOn "2016-02-19"^^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:NP646113.RAjbx2Wrw40UMZDS8_FST_8oTxNkTS9fQxTQZOqdwn53I130_publicationInfo {
  this: dcterms:created "2016-05-13T12:46:38+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: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 "v4.0.0.0" .
  
  dgn-void:disgenetv3.0rdf pav:version "v4.0.0" .
}