@prefix this: <http://rdf.disgenet.org/resource/nanopub/NP523330.RA2P27gvHeLW3T-Mey54VmFHzIXdqEsDpO1LKzFItVkH0> .
@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:NP523330.RA2P27gvHeLW3T-Mey54VmFHzIXdqEsDpO1LKzFItVkH0130_head {
  this: np:hasAssertion dgn-np:NP523330.RA2P27gvHeLW3T-Mey54VmFHzIXdqEsDpO1LKzFItVkH0130_assertion;
    np:hasProvenance dgn-np:NP523330.RA2P27gvHeLW3T-Mey54VmFHzIXdqEsDpO1LKzFItVkH0130_provenance;
    np:hasPublicationInfo dgn-np:NP523330.RA2P27gvHeLW3T-Mey54VmFHzIXdqEsDpO1LKzFItVkH0130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP523330.RA2P27gvHeLW3T-Mey54VmFHzIXdqEsDpO1LKzFItVkH0130_assertion a np:Assertion .
  
  dgn-np:NP523330.RA2P27gvHeLW3T-Mey54VmFHzIXdqEsDpO1LKzFItVkH0130_provenance a np:Provenance .
  
  dgn-np:NP523330.RA2P27gvHeLW3T-Mey54VmFHzIXdqEsDpO1LKzFItVkH0130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP523330.RA2P27gvHeLW3T-Mey54VmFHzIXdqEsDpO1LKzFItVkH0130_assertion {
  miriam-gene:1956 a ncit:C16612 .
  
  lld:C1168401 a ncit:C7057 .
  
  dgn-gda:DGN8a302ba1bed12e71fdc6aa41275915d8 sio:SIO_000628 miriam-gene:1956, lld:C1168401;
    a sio:SIO_001121 .
}

dgn-np:NP523330.RA2P27gvHeLW3T-Mey54VmFHzIXdqEsDpO1LKzFItVkH0130_provenance {
  dgn-np:NP523330.RA2P27gvHeLW3T-Mey54VmFHzIXdqEsDpO1LKzFItVkH0130_assertion dcterms:description
      "[Our data indicate that unlike NSCLC, EGFR kinase mutations are rare in unselected cases of SCCHN within the United States and are not linked to gefitinib or erlotinib responses in SCCHN.]. 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:16299242;
    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:NP523330.RA2P27gvHeLW3T-Mey54VmFHzIXdqEsDpO1LKzFItVkH0130_publicationInfo {
  this: dcterms:created "2016-05-13T12:45:42+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" .
}