@prefix this: <http://rdf.disgenet.org/resource/nanopub/NP1302299.RA_pcIOOY97I4yXCada0mJsh9IIuwITKe9zS9pWcb97jU> .
@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:NP1302299.RA_pcIOOY97I4yXCada0mJsh9IIuwITKe9zS9pWcb97jU130_head {
  this: np:hasAssertion dgn-np:NP1302299.RA_pcIOOY97I4yXCada0mJsh9IIuwITKe9zS9pWcb97jU130_assertion;
    np:hasProvenance dgn-np:NP1302299.RA_pcIOOY97I4yXCada0mJsh9IIuwITKe9zS9pWcb97jU130_provenance;
    np:hasPublicationInfo dgn-np:NP1302299.RA_pcIOOY97I4yXCada0mJsh9IIuwITKe9zS9pWcb97jU130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP1302299.RA_pcIOOY97I4yXCada0mJsh9IIuwITKe9zS9pWcb97jU130_assertion a np:Assertion .
  
  dgn-np:NP1302299.RA_pcIOOY97I4yXCada0mJsh9IIuwITKe9zS9pWcb97jU130_provenance a np:Provenance .
  
  dgn-np:NP1302299.RA_pcIOOY97I4yXCada0mJsh9IIuwITKe9zS9pWcb97jU130_publicationInfo
    a np:PublicationInfo .
}

dgn-np:NP1302299.RA_pcIOOY97I4yXCada0mJsh9IIuwITKe9zS9pWcb97jU130_assertion {
  miriam-gene:1956 a ncit:C16612 .
  
  lld:C0017638 a ncit:C7057 .
  
  dgn-gda:DGNa58fe2c6e2fcee0df6100764d0f9fbeb sio:SIO_000628 miriam-gene:1956, lld:C0017638;
    a sio:SIO_001121 .
}

dgn-np:NP1302299.RA_pcIOOY97I4yXCada0mJsh9IIuwITKe9zS9pWcb97jU130_provenance {
  dgn-np:NP1302299.RA_pcIOOY97I4yXCada0mJsh9IIuwITKe9zS9pWcb97jU130_assertion dcterms:description
      "[These studies suggest that DM are the usual locus for amplified genes (usually EGFR) in human glioma biopsies, but that structural abnormalities of 7p may be associated with EGFR amplification in a small proportion of these tumors.]. 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:3478127;
    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:NP1302299.RA_pcIOOY97I4yXCada0mJsh9IIuwITKe9zS9pWcb97jU130_publicationInfo {
  this: dcterms:created "2016-05-13T12:51:36+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" .
}