@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP350816.RAM8Is2qZr_q6AOZIgnn8RjrVH2hnqcEPS7O22rJkrNXE> .
@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:NP350816.RAM8Is2qZr_q6AOZIgnn8RjrVH2hnqcEPS7O22rJkrNXE130_head {
  this: np:hasAssertion dgn-np:NP350816.RAM8Is2qZr_q6AOZIgnn8RjrVH2hnqcEPS7O22rJkrNXE130_assertion;
    np:hasProvenance dgn-np:NP350816.RAM8Is2qZr_q6AOZIgnn8RjrVH2hnqcEPS7O22rJkrNXE130_provenance;
    np:hasPublicationInfo dgn-np:NP350816.RAM8Is2qZr_q6AOZIgnn8RjrVH2hnqcEPS7O22rJkrNXE130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP350816.RAM8Is2qZr_q6AOZIgnn8RjrVH2hnqcEPS7O22rJkrNXE130_assertion a np:Assertion .
  
  dgn-np:NP350816.RAM8Is2qZr_q6AOZIgnn8RjrVH2hnqcEPS7O22rJkrNXE130_provenance a np:Provenance .
  
  dgn-np:NP350816.RAM8Is2qZr_q6AOZIgnn8RjrVH2hnqcEPS7O22rJkrNXE130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP350816.RAM8Is2qZr_q6AOZIgnn8RjrVH2hnqcEPS7O22rJkrNXE130_assertion {
  miriam-gene:7294 a ncit:C16612 .
  
  lld:C0242379 a ncit:C7057 .
  
  dgn-gda:DGN256e4fe7950b6fe69e37b827cced45a8 sio:SIO_000628 miriam-gene:7294, lld:C0242379;
    a sio:SIO_001121 .
}

dgn-np:NP350816.RAM8Is2qZr_q6AOZIgnn8RjrVH2hnqcEPS7O22rJkrNXE130_provenance {
  dgn-np:NP350816.RAM8Is2qZr_q6AOZIgnn8RjrVH2hnqcEPS7O22rJkrNXE130_assertion dcterms:description
      "[Somatic mutations in the tyrosine kinase (TK) domain of the epidermal growth factor receptor (EGFR) gene in lung cancers have generated enormous interest, because they predict for sensitivity to TK inhibitors (TKIs).]. 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:16231326;
    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:NP350816.RAM8Is2qZr_q6AOZIgnn8RjrVH2hnqcEPS7O22rJkrNXE130_publicationInfo {
  this: dcterms:created "2014-10-02T12:35:26+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" .
}