@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP739966.RAYy2ek5tFoJ8qM0923ZgIjoB9mhjtPbofiClNXP3vfwc> .
@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:NP739966.RAYy2ek5tFoJ8qM0923ZgIjoB9mhjtPbofiClNXP3vfwc130_head {
  this: np:hasAssertion dgn-np:NP739966.RAYy2ek5tFoJ8qM0923ZgIjoB9mhjtPbofiClNXP3vfwc130_assertion ;
    np:hasProvenance dgn-np:NP739966.RAYy2ek5tFoJ8qM0923ZgIjoB9mhjtPbofiClNXP3vfwc130_provenance ;
    np:hasPublicationInfo dgn-np:NP739966.RAYy2ek5tFoJ8qM0923ZgIjoB9mhjtPbofiClNXP3vfwc130_publicationInfo ;
    a np:Nanopublication .
  dgn-np:NP739966.RAYy2ek5tFoJ8qM0923ZgIjoB9mhjtPbofiClNXP3vfwc130_assertion a np:Assertion .
  dgn-np:NP739966.RAYy2ek5tFoJ8qM0923ZgIjoB9mhjtPbofiClNXP3vfwc130_provenance a np:Provenance .
  dgn-np:NP739966.RAYy2ek5tFoJ8qM0923ZgIjoB9mhjtPbofiClNXP3vfwc130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP739966.RAYy2ek5tFoJ8qM0923ZgIjoB9mhjtPbofiClNXP3vfwc130_assertion {
  miriam-gene:3394 a ncit:C16612 .
  lld:C2931822 a ncit:C7057 .
  dgn-gda:DGNa9713349c52d3506f191b380f5507f53 sio:SIO_000628 miriam-gene:3394 , lld:C2931822 ;
    a sio:SIO_001121 .
}
dgn-np:NP739966.RAYy2ek5tFoJ8qM0923ZgIjoB9mhjtPbofiClNXP3vfwc130_provenance {
  dgn-np:NP739966.RAYy2ek5tFoJ8qM0923ZgIjoB9mhjtPbofiClNXP3vfwc130_assertion dcterms:description "[In contrast to the broad expression of IRF8 in normal adult and fetal tissues, transcriptional silencing and promoter methylation of IRF8 were frequently detected in multiple carcinoma (except for hepatocellular) cell lines (100% in NPC, 88% in esophageal and 18-78% in other carcinoma cell lines) and in a large collection of primary carcinomas (78% in NPC, 36-71% in other carcinomas).]. 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:18469857 ;
    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:NP739966.RAYy2ek5tFoJ8qM0923ZgIjoB9mhjtPbofiClNXP3vfwc130_publicationInfo {
  this: dcterms:created "2014-10-02T12:39:29+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" .
}