@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP515692.RAQywD3ynkRkxKyeNUYee9sOV63ROLCLkVq1mud7lGtj4> .
@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:NP515692.RAQywD3ynkRkxKyeNUYee9sOV63ROLCLkVq1mud7lGtj4130_head {
  this: np:hasAssertion dgn-np:NP515692.RAQywD3ynkRkxKyeNUYee9sOV63ROLCLkVq1mud7lGtj4130_assertion ;
    np:hasProvenance dgn-np:NP515692.RAQywD3ynkRkxKyeNUYee9sOV63ROLCLkVq1mud7lGtj4130_provenance ;
    np:hasPublicationInfo dgn-np:NP515692.RAQywD3ynkRkxKyeNUYee9sOV63ROLCLkVq1mud7lGtj4130_publicationInfo ;
    a np:Nanopublication .
  dgn-np:NP515692.RAQywD3ynkRkxKyeNUYee9sOV63ROLCLkVq1mud7lGtj4130_assertion a np:Assertion .
  dgn-np:NP515692.RAQywD3ynkRkxKyeNUYee9sOV63ROLCLkVq1mud7lGtj4130_provenance a np:Provenance .
  dgn-np:NP515692.RAQywD3ynkRkxKyeNUYee9sOV63ROLCLkVq1mud7lGtj4130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP515692.RAQywD3ynkRkxKyeNUYee9sOV63ROLCLkVq1mud7lGtj4130_assertion {
  miriam-gene:81031 a ncit:C16612 .
  lld:C0729233 a ncit:C7057 .
  dgn-gda:DGN00177782cdf7063aaa4b03c369933547 sio:SIO_000628 miriam-gene:81031 , lld:C0729233 ;
    a sio:SIO_001121 .
}
dgn-np:NP515692.RAQywD3ynkRkxKyeNUYee9sOV63ROLCLkVq1mud7lGtj4130_provenance {
  dgn-np:NP515692.RAQywD3ynkRkxKyeNUYee9sOV63ROLCLkVq1mud7lGtj4130_assertion dcterms:description "[To retrospectively identify quantitative computed tomographic (CT) features that correlate with epidermal growth factor receptor (EGFR) mutation in surgically resected lung adenocarcinomas stratified by the International Association for the Study of Lung Cancer (IASLC), American Thoracic Society (ATS), and European Respiratory Society (ERS) classification in an East Asian cohort of patients known to have a high prevalence of EGFR mutations.]. 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:23468578 ;
    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:NP515692.RAQywD3ynkRkxKyeNUYee9sOV63ROLCLkVq1mud7lGtj4130_publicationInfo {
  this: dcterms:created "2014-10-02T12:37:07+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" .
}