@prefix this: <http://rdf.disgenet.org/resource/nanopub/NP410453.RAcSXGPkzKoF10gz3Wd2Fcugb5qWh1sx1xGlDb7XHaiXM> .
@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:NP410453.RAcSXGPkzKoF10gz3Wd2Fcugb5qWh1sx1xGlDb7XHaiXM130_head {
  this: np:hasAssertion dgn-np:NP410453.RAcSXGPkzKoF10gz3Wd2Fcugb5qWh1sx1xGlDb7XHaiXM130_assertion;
    np:hasProvenance dgn-np:NP410453.RAcSXGPkzKoF10gz3Wd2Fcugb5qWh1sx1xGlDb7XHaiXM130_provenance;
    np:hasPublicationInfo dgn-np:NP410453.RAcSXGPkzKoF10gz3Wd2Fcugb5qWh1sx1xGlDb7XHaiXM130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP410453.RAcSXGPkzKoF10gz3Wd2Fcugb5qWh1sx1xGlDb7XHaiXM130_assertion a np:Assertion .
  
  dgn-np:NP410453.RAcSXGPkzKoF10gz3Wd2Fcugb5qWh1sx1xGlDb7XHaiXM130_provenance a np:Provenance .
  
  dgn-np:NP410453.RAcSXGPkzKoF10gz3Wd2Fcugb5qWh1sx1xGlDb7XHaiXM130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP410453.RAcSXGPkzKoF10gz3Wd2Fcugb5qWh1sx1xGlDb7XHaiXM130_assertion {
  miriam-gene:1956 a ncit:C16612 .
  
  lld:C0017636 a ncit:C7057 .
  
  dgn-gda:DGNbd440486175e33546746115e0c63c237 sio:SIO_000628 miriam-gene:1956, lld:C0017636;
    a sio:SIO_001121 .
}

dgn-np:NP410453.RAcSXGPkzKoF10gz3Wd2Fcugb5qWh1sx1xGlDb7XHaiXM130_provenance {
  dgn-np:NP410453.RAcSXGPkzKoF10gz3Wd2Fcugb5qWh1sx1xGlDb7XHaiXM130_assertion dcterms:description
      "[The loss of sequences on chromosome 10 and the deletions of 9p (that is loss of tumor suppressor genes on these locations), and epidermal growth factor receptor gene amplification, have been proposed as sequential abnormalities participating in glioblastoma tumorigenesis.]. 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:1336685;
    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:NP410453.RAcSXGPkzKoF10gz3Wd2Fcugb5qWh1sx1xGlDb7XHaiXM130_publicationInfo {
  this: dcterms:created "2016-05-13T12:44:51+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" .
}