@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP541439.RAenVTFaeNmgfeDBjEuOaAjZmZhlxzi8123cO7mJVqU5c> .
@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:NP541439.RAenVTFaeNmgfeDBjEuOaAjZmZhlxzi8123cO7mJVqU5c130_head {
  this: np:hasAssertion dgn-np:NP541439.RAenVTFaeNmgfeDBjEuOaAjZmZhlxzi8123cO7mJVqU5c130_assertion;
    np:hasProvenance dgn-np:NP541439.RAenVTFaeNmgfeDBjEuOaAjZmZhlxzi8123cO7mJVqU5c130_provenance;
    np:hasPublicationInfo dgn-np:NP541439.RAenVTFaeNmgfeDBjEuOaAjZmZhlxzi8123cO7mJVqU5c130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP541439.RAenVTFaeNmgfeDBjEuOaAjZmZhlxzi8123cO7mJVqU5c130_assertion a np:Assertion .
  
  dgn-np:NP541439.RAenVTFaeNmgfeDBjEuOaAjZmZhlxzi8123cO7mJVqU5c130_provenance a np:Provenance .
  
  dgn-np:NP541439.RAenVTFaeNmgfeDBjEuOaAjZmZhlxzi8123cO7mJVqU5c130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP541439.RAenVTFaeNmgfeDBjEuOaAjZmZhlxzi8123cO7mJVqU5c130_assertion {
  miriam-gene:3845 a ncit:C16612 .
  
  lld:C0007137 a ncit:C7057 .
  
  dgn-gda:DGN74e64ee9fd516f8dc97f259580d0aabe sio:SIO_000628 miriam-gene:3845, lld:C0007137;
    a sio:SIO_001121 .
}

dgn-np:NP541439.RAenVTFaeNmgfeDBjEuOaAjZmZhlxzi8123cO7mJVqU5c130_provenance {
  dgn-np:NP541439.RAenVTFaeNmgfeDBjEuOaAjZmZhlxzi8123cO7mJVqU5c130_assertion dcterms:description
      "[The aim of the study was to analyze EGFR expression and KRAS and EGFR mutational status and to correlate it with treatment response to anti-EGFR therapy combined with radiotherapy in 29 patients with advanced head and neck squamous cell carcinomas (HNSCC).EGFR gene expression normalized to GAPDH and EGFR variant type III (EGFRvIII) was detected in tumor tissue using real time reverse transcription -PCR.]. 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:22668015;
    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:NP541439.RAenVTFaeNmgfeDBjEuOaAjZmZhlxzi8123cO7mJVqU5c130_publicationInfo {
  this: dcterms:created "2014-10-02T12:37:27+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" .
}