@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP440486.RAWJbRJKEpkElHdzdIGAubzoyhSbzXDOhOGPh43rW_5Rk> .
@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:NP440486.RAWJbRJKEpkElHdzdIGAubzoyhSbzXDOhOGPh43rW_5Rk130_head {
  this: np:hasAssertion dgn-np:NP440486.RAWJbRJKEpkElHdzdIGAubzoyhSbzXDOhOGPh43rW_5Rk130_assertion ;
    np:hasProvenance dgn-np:NP440486.RAWJbRJKEpkElHdzdIGAubzoyhSbzXDOhOGPh43rW_5Rk130_provenance ;
    np:hasPublicationInfo dgn-np:NP440486.RAWJbRJKEpkElHdzdIGAubzoyhSbzXDOhOGPh43rW_5Rk130_publicationInfo ;
    a np:Nanopublication .
  dgn-np:NP440486.RAWJbRJKEpkElHdzdIGAubzoyhSbzXDOhOGPh43rW_5Rk130_assertion a np:Assertion .
  dgn-np:NP440486.RAWJbRJKEpkElHdzdIGAubzoyhSbzXDOhOGPh43rW_5Rk130_provenance a np:Provenance .
  dgn-np:NP440486.RAWJbRJKEpkElHdzdIGAubzoyhSbzXDOhOGPh43rW_5Rk130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP440486.RAWJbRJKEpkElHdzdIGAubzoyhSbzXDOhOGPh43rW_5Rk130_assertion {
  miriam-gene:1956 a ncit:C16612 .
  lld:C0238461 a ncit:C7057 .
  dgn-gda:DGN75270005046e993d4bffac0c3dc9872b sio:SIO_000628 miriam-gene:1956 , lld:C0238461 ;
    a sio:SIO_001121 .
}
dgn-np:NP440486.RAWJbRJKEpkElHdzdIGAubzoyhSbzXDOhOGPh43rW_5Rk130_provenance {
  dgn-np:NP440486.RAWJbRJKEpkElHdzdIGAubzoyhSbzXDOhOGPh43rW_5Rk130_assertion dcterms:description "[Despite the low incidence of somatic EGFR gene mutation and amplification in the study samples, in view of the fact that high polysomy was often identified by FISH, as well as the current lack of therapeutic options, EGFR TKIs are worth investigating for treating the patients with ATC who have at least giant cell subtype.]. 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:17079354 ;
    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:NP440486.RAWJbRJKEpkElHdzdIGAubzoyhSbzXDOhOGPh43rW_5Rk130_publicationInfo {
  this: dcterms:created "2014-10-02T12:36:20+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" .
}