@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP583277.RA6fmELnz6fEAtlzdAfHEBn4xaFnb99XlQZXBlU7Id-hk> .
@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:NP583277.RA6fmELnz6fEAtlzdAfHEBn4xaFnb99XlQZXBlU7Id-hk130_head {
  this: np:hasAssertion dgn-np:NP583277.RA6fmELnz6fEAtlzdAfHEBn4xaFnb99XlQZXBlU7Id-hk130_assertion ;
    np:hasProvenance dgn-np:NP583277.RA6fmELnz6fEAtlzdAfHEBn4xaFnb99XlQZXBlU7Id-hk130_provenance ;
    np:hasPublicationInfo dgn-np:NP583277.RA6fmELnz6fEAtlzdAfHEBn4xaFnb99XlQZXBlU7Id-hk130_publicationInfo ;
    a np:Nanopublication .
  dgn-np:NP583277.RA6fmELnz6fEAtlzdAfHEBn4xaFnb99XlQZXBlU7Id-hk130_assertion a np:Assertion .
  dgn-np:NP583277.RA6fmELnz6fEAtlzdAfHEBn4xaFnb99XlQZXBlU7Id-hk130_provenance a np:Provenance .
  dgn-np:NP583277.RA6fmELnz6fEAtlzdAfHEBn4xaFnb99XlQZXBlU7Id-hk130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP583277.RA6fmELnz6fEAtlzdAfHEBn4xaFnb99XlQZXBlU7Id-hk130_assertion {
  miriam-gene:54361 a ncit:C16612 .
  lld:C0242379 a ncit:C7057 .
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    a sio:SIO_001121 .
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dgn-np:NP583277.RA6fmELnz6fEAtlzdAfHEBn4xaFnb99XlQZXBlU7Id-hk130_provenance {
  dgn-np:NP583277.RA6fmELnz6fEAtlzdAfHEBn4xaFnb99XlQZXBlU7Id-hk130_assertion dcterms:description "[Our finding of a 0.4 Mb amplified region at 1p36.12 containing WNT4 in preinvasive lung cancer, coupled with the identification of three additional alterations in invasive tumors that also contain genes related to the Notch and Wnt pathways, strongly suggests an intricate role of these pathways in early and late stages of lung cancer development.]. 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:15615770 ;
    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:NP583277.RA6fmELnz6fEAtlzdAfHEBn4xaFnb99XlQZXBlU7Id-hk130_publicationInfo {
  this: dcterms:created "2014-10-02T12:37:51+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 ;
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    pav:createdBy <http://orcid.org/0000-0003-0169-8159> ;
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}