@prefix this: <http://rdf.disgenet.org/resource/nanopub/NP1042639.RAJG1L5vyDVfGZU7r_nAv3dQXgeJTgIGTo9W2wix8vS1Q> .
@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:NP1042639.RAJG1L5vyDVfGZU7r_nAv3dQXgeJTgIGTo9W2wix8vS1Q130_head {
  this: np:hasAssertion dgn-np:NP1042639.RAJG1L5vyDVfGZU7r_nAv3dQXgeJTgIGTo9W2wix8vS1Q130_assertion;
    np:hasProvenance dgn-np:NP1042639.RAJG1L5vyDVfGZU7r_nAv3dQXgeJTgIGTo9W2wix8vS1Q130_provenance;
    np:hasPublicationInfo dgn-np:NP1042639.RAJG1L5vyDVfGZU7r_nAv3dQXgeJTgIGTo9W2wix8vS1Q130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP1042639.RAJG1L5vyDVfGZU7r_nAv3dQXgeJTgIGTo9W2wix8vS1Q130_assertion a np:Assertion .
  
  dgn-np:NP1042639.RAJG1L5vyDVfGZU7r_nAv3dQXgeJTgIGTo9W2wix8vS1Q130_provenance a np:Provenance .
  
  dgn-np:NP1042639.RAJG1L5vyDVfGZU7r_nAv3dQXgeJTgIGTo9W2wix8vS1Q130_publicationInfo
    a np:PublicationInfo .
}

dgn-np:NP1042639.RAJG1L5vyDVfGZU7r_nAv3dQXgeJTgIGTo9W2wix8vS1Q130_assertion {
  miriam-gene:238 a ncit:C16612 .
  
  lld:C0242379 a ncit:C7057 .
  
  dgn-gda:DGN5a3e9896aa2c0ed39fe06e75aeb66b16 sio:SIO_000628 miriam-gene:238, lld:C0242379;
    a sio:SIO_001121 .
}

dgn-np:NP1042639.RAJG1L5vyDVfGZU7r_nAv3dQXgeJTgIGTo9W2wix8vS1Q130_provenance {
  dgn-np:NP1042639.RAJG1L5vyDVfGZU7r_nAv3dQXgeJTgIGTo9W2wix8vS1Q130_assertion dcterms:description
      "[Epidermal growth factor (EGF) receptor (EGFR) mutations are the best illustration of the therapeutic relevance of identifying such molecular clusters of lung cancer based on driver genetic alterations that predict the efficacy of specific tyrosine kinase inhibitors, a strategy referred to as personalized medicine. Besides EGFR and ALK, other genes harboring driver molecular alterations have been identified as part of integrated genomic studies of lung cancers.]. 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:23307186;
    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:NP1042639.RAJG1L5vyDVfGZU7r_nAv3dQXgeJTgIGTo9W2wix8vS1Q130_publicationInfo {
  this: dcterms:created "2016-05-13T12:49:38+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" .
}