@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP172138.RAkeLPZ4IsUrNxwasdxKmsNPpfnDvuFOOmBYnqqHwWWsA> .
@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:NP172138.RAkeLPZ4IsUrNxwasdxKmsNPpfnDvuFOOmBYnqqHwWWsA130_head {
  this: np:hasAssertion dgn-np:NP172138.RAkeLPZ4IsUrNxwasdxKmsNPpfnDvuFOOmBYnqqHwWWsA130_assertion ;
    np:hasProvenance dgn-np:NP172138.RAkeLPZ4IsUrNxwasdxKmsNPpfnDvuFOOmBYnqqHwWWsA130_provenance ;
    np:hasPublicationInfo dgn-np:NP172138.RAkeLPZ4IsUrNxwasdxKmsNPpfnDvuFOOmBYnqqHwWWsA130_publicationInfo ;
    a np:Nanopublication .
  dgn-np:NP172138.RAkeLPZ4IsUrNxwasdxKmsNPpfnDvuFOOmBYnqqHwWWsA130_assertion a np:Assertion .
  dgn-np:NP172138.RAkeLPZ4IsUrNxwasdxKmsNPpfnDvuFOOmBYnqqHwWWsA130_provenance a np:Provenance .
  dgn-np:NP172138.RAkeLPZ4IsUrNxwasdxKmsNPpfnDvuFOOmBYnqqHwWWsA130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP172138.RAkeLPZ4IsUrNxwasdxKmsNPpfnDvuFOOmBYnqqHwWWsA130_assertion {
  miriam-gene:64689 a ncit:C16612 .
  lld:C1168401 a ncit:C7057 .
  dgn-gda:DGNe895e7dc191498af8bdccd4223cf7b0d sio:SIO_000628 miriam-gene:64689 , lld:C1168401 ;
    a sio:SIO_001121 .
}
dgn-np:NP172138.RAkeLPZ4IsUrNxwasdxKmsNPpfnDvuFOOmBYnqqHwWWsA130_provenance {
  dgn-np:NP172138.RAkeLPZ4IsUrNxwasdxKmsNPpfnDvuFOOmBYnqqHwWWsA130_assertion dcterms:description "[To infer relevant and specific pathway activation downstream of EGFR from gene expression in HNSCC, we generated gene expression signatures using immortalized keratinocytes (HaCaT) subjected to ligand stimulation and transfected with EGFR, RELA/p65, or HRASVal12D.]. 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:22549044 ;
    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:NP172138.RAkeLPZ4IsUrNxwasdxKmsNPpfnDvuFOOmBYnqqHwWWsA130_publicationInfo {
  this: dcterms:created "2014-10-02T12:33:33+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 ;
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    pav:createdBy <http://orcid.org/0000-0003-0169-8159> ;
    pav:version "v2.1.0.0" .
  dgn-void:disgenetrdf pav:version "v2.1.0" .
}