@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP511992.RAmUxO-l0NwupzmSPfrmrU09SJD6OIwQPafaqAjp2BZcQ> .
@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:NP511992.RAmUxO-l0NwupzmSPfrmrU09SJD6OIwQPafaqAjp2BZcQ130_head {
  this: np:hasAssertion dgn-np:NP511992.RAmUxO-l0NwupzmSPfrmrU09SJD6OIwQPafaqAjp2BZcQ130_assertion ;
    np:hasProvenance dgn-np:NP511992.RAmUxO-l0NwupzmSPfrmrU09SJD6OIwQPafaqAjp2BZcQ130_provenance ;
    np:hasPublicationInfo dgn-np:NP511992.RAmUxO-l0NwupzmSPfrmrU09SJD6OIwQPafaqAjp2BZcQ130_publicationInfo ;
    a np:Nanopublication .
  dgn-np:NP511992.RAmUxO-l0NwupzmSPfrmrU09SJD6OIwQPafaqAjp2BZcQ130_assertion a np:Assertion .
  dgn-np:NP511992.RAmUxO-l0NwupzmSPfrmrU09SJD6OIwQPafaqAjp2BZcQ130_provenance a np:Provenance .
  dgn-np:NP511992.RAmUxO-l0NwupzmSPfrmrU09SJD6OIwQPafaqAjp2BZcQ130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP511992.RAmUxO-l0NwupzmSPfrmrU09SJD6OIwQPafaqAjp2BZcQ130_assertion {
  miriam-gene:8626 a ncit:C16612 .
  lld:C0242379 a ncit:C7057 .
  dgn-gda:DGN14c362af2621ca244937bff4c3fe045b sio:SIO_000628 miriam-gene:8626 , lld:C0242379 ;
    a sio:SIO_001121 .
}
dgn-np:NP511992.RAmUxO-l0NwupzmSPfrmrU09SJD6OIwQPafaqAjp2BZcQ130_provenance {
  dgn-np:NP511992.RAmUxO-l0NwupzmSPfrmrU09SJD6OIwQPafaqAjp2BZcQ130_assertion dcterms:description "[These results, taken together with previous reports of oncogenic alterations of transcription factors involved in lung development (p63, CEBPA), suggest genetic alterations that directly interfere with transcriptional networks normally regulating lung development may be a more common feature of lung cancer than previously realized.]. 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:17925434 ;
    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:NP511992.RAmUxO-l0NwupzmSPfrmrU09SJD6OIwQPafaqAjp2BZcQ130_publicationInfo {
  this: dcterms:created "2014-10-02T12:37:05+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" .
}