@prefix this: <http://rdf.disgenet.org/resource/nanopub/NP572782.RAOfcFN5TAedK84-i-HtuLdLpl9C0vWq4ZRxMtpz3e-p8> .
@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:NP572782.RAOfcFN5TAedK84-i-HtuLdLpl9C0vWq4ZRxMtpz3e-p8130_head {
  this: np:hasAssertion dgn-np:NP572782.RAOfcFN5TAedK84-i-HtuLdLpl9C0vWq4ZRxMtpz3e-p8130_assertion;
    np:hasProvenance dgn-np:NP572782.RAOfcFN5TAedK84-i-HtuLdLpl9C0vWq4ZRxMtpz3e-p8130_provenance;
    np:hasPublicationInfo dgn-np:NP572782.RAOfcFN5TAedK84-i-HtuLdLpl9C0vWq4ZRxMtpz3e-p8130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP572782.RAOfcFN5TAedK84-i-HtuLdLpl9C0vWq4ZRxMtpz3e-p8130_assertion a np:Assertion .
  
  dgn-np:NP572782.RAOfcFN5TAedK84-i-HtuLdLpl9C0vWq4ZRxMtpz3e-p8130_provenance a np:Provenance .
  
  dgn-np:NP572782.RAOfcFN5TAedK84-i-HtuLdLpl9C0vWq4ZRxMtpz3e-p8130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP572782.RAOfcFN5TAedK84-i-HtuLdLpl9C0vWq4ZRxMtpz3e-p8130_assertion {
  miriam-gene:1956 a ncit:C16612 .
  
  lld:C0007131 a ncit:C7057 .
  
  dgn-gda:DGNbfc8587cce4fb957730ba0a8bd8afd62 sio:SIO_000628 miriam-gene:1956, lld:C0007131;
    a sio:SIO_001121 .
}

dgn-np:NP572782.RAOfcFN5TAedK84-i-HtuLdLpl9C0vWq4ZRxMtpz3e-p8130_provenance {
  dgn-np:NP572782.RAOfcFN5TAedK84-i-HtuLdLpl9C0vWq4ZRxMtpz3e-p8130_assertion dcterms:description
      "[Thus, understanding how activating mutations in the TKD domain of EGFR contribute to radiosensitivity should provide new insight into effective treatment of NSCLC with radiotherapy and perhaps avoid emergence of single agent drug resistance.]. 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:17018617;
    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:NP572782.RAOfcFN5TAedK84-i-HtuLdLpl9C0vWq4ZRxMtpz3e-p8130_publicationInfo {
  this: dcterms:created "2016-05-13T12:46:04+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" .
}