@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP163489.RATx8j_vtSzQGxAkjngEffKZktQjFuv3MDS8VFC8kUne8> .
@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:NP163489.RATx8j_vtSzQGxAkjngEffKZktQjFuv3MDS8VFC8kUne8130_head {
  this: np:hasAssertion dgn-np:NP163489.RATx8j_vtSzQGxAkjngEffKZktQjFuv3MDS8VFC8kUne8130_assertion;
    np:hasProvenance dgn-np:NP163489.RATx8j_vtSzQGxAkjngEffKZktQjFuv3MDS8VFC8kUne8130_provenance;
    np:hasPublicationInfo dgn-np:NP163489.RATx8j_vtSzQGxAkjngEffKZktQjFuv3MDS8VFC8kUne8130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP163489.RATx8j_vtSzQGxAkjngEffKZktQjFuv3MDS8VFC8kUne8130_assertion a np:Assertion .
  
  dgn-np:NP163489.RATx8j_vtSzQGxAkjngEffKZktQjFuv3MDS8VFC8kUne8130_provenance a np:Provenance .
  
  dgn-np:NP163489.RATx8j_vtSzQGxAkjngEffKZktQjFuv3MDS8VFC8kUne8130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP163489.RATx8j_vtSzQGxAkjngEffKZktQjFuv3MDS8VFC8kUne8130_assertion {
  miriam-gene:1956 a ncit:C16612 .
  
  lld:C0242379 a ncit:C7057 .
  
  dgn-gda:DGN44b1c15d719b37a9c25ac41b78d39bbd sio:SIO_000628 miriam-gene:1956, lld:C0242379;
    a sio:SIO_001121 .
}

dgn-np:NP163489.RATx8j_vtSzQGxAkjngEffKZktQjFuv3MDS8VFC8kUne8130_provenance {
  dgn-np:NP163489.RATx8j_vtSzQGxAkjngEffKZktQjFuv3MDS8VFC8kUne8130_assertion dcterms:description
      "[The current study further demonstrates that a double genetic event in EGFR can occasionally occur in lung cancer, thus providing new clues for understanding the involvement of epidermal growth factor receptor signaling cascades in the pathogenesis of NSCLC.]. 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:16863509;
    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:NP163489.RATx8j_vtSzQGxAkjngEffKZktQjFuv3MDS8VFC8kUne8130_publicationInfo {
  this: dcterms:created "2014-10-02T12:33:28+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" .
}