@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP337937.RAvfhiwqlYMJ1NDZXnoL3XGaM9oTdv3FW1VmvvM_hwix0> .
@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#> .

dgn-np:NP337937.RAvfhiwqlYMJ1NDZXnoL3XGaM9oTdv3FW1VmvvM_hwix0130_head {
  this: np:hasAssertion dgn-np:NP337937.RAvfhiwqlYMJ1NDZXnoL3XGaM9oTdv3FW1VmvvM_hwix0130_assertion;
    np:hasProvenance dgn-np:NP337937.RAvfhiwqlYMJ1NDZXnoL3XGaM9oTdv3FW1VmvvM_hwix0130_provenance;
    np:hasPublicationInfo dgn-np:NP337937.RAvfhiwqlYMJ1NDZXnoL3XGaM9oTdv3FW1VmvvM_hwix0130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP337937.RAvfhiwqlYMJ1NDZXnoL3XGaM9oTdv3FW1VmvvM_hwix0130_assertion a np:Assertion .
  
  dgn-np:NP337937.RAvfhiwqlYMJ1NDZXnoL3XGaM9oTdv3FW1VmvvM_hwix0130_provenance a np:Provenance .
  
  dgn-np:NP337937.RAvfhiwqlYMJ1NDZXnoL3XGaM9oTdv3FW1VmvvM_hwix0130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP337937.RAvfhiwqlYMJ1NDZXnoL3XGaM9oTdv3FW1VmvvM_hwix0130_assertion {
  miriam-gene:1956 a ncit:C16612 .
  
  lld:C0205851 a ncit:C7057 .
  
  dgn-gda:DGN451e818a9d85cca351c76db36de9b6cd sio:SIO_000628 miriam-gene:1956, lld:C0205851;
    a sio:SIO_001121 .
}

dgn-np:NP337937.RAvfhiwqlYMJ1NDZXnoL3XGaM9oTdv3FW1VmvvM_hwix0130_provenance {
  dgn-np:NP337937.RAvfhiwqlYMJ1NDZXnoL3XGaM9oTdv3FW1VmvvM_hwix0130_assertion dcterms:description
      "[These results suggest that overexpression of EGFR protein and increased copy number or amplification of the EGFR gene occur relatively frequently in primary TGCTs, and may play roles in the formation of invasive cancer and in the progression, especially morphological evolution, of 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:20608935;
    prov:wasDerivedFrom dgn-void:befree-20140225;
    prov:wasGeneratedBy eco:ECO_0000203 .
  
  dgn-void:befree-20140225 pav:importedOn "2014-02-25"^^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:NP337937.RAvfhiwqlYMJ1NDZXnoL3XGaM9oTdv3FW1VmvvM_hwix0130_publicationInfo {
  this: dcterms:created "2014-10-02T12:35:19+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:disgenetrdf;
    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 "v2.1.0.0" .
  
  dgn-void:disgenetrdf pav:version "v2.1.0" .
}