@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP86035.RAmeQMzkg67X5TS_GtJLIyunZQS8SkWX-tz3Kk2O21caE> .
@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:NP86035.RAmeQMzkg67X5TS_GtJLIyunZQS8SkWX-tz3Kk2O21caE130_head {
  this: np:hasAssertion dgn-np:NP86035.RAmeQMzkg67X5TS_GtJLIyunZQS8SkWX-tz3Kk2O21caE130_assertion ;
    np:hasProvenance dgn-np:NP86035.RAmeQMzkg67X5TS_GtJLIyunZQS8SkWX-tz3Kk2O21caE130_provenance ;
    np:hasPublicationInfo dgn-np:NP86035.RAmeQMzkg67X5TS_GtJLIyunZQS8SkWX-tz3Kk2O21caE130_publicationInfo ;
    a np:Nanopublication .
  dgn-np:NP86035.RAmeQMzkg67X5TS_GtJLIyunZQS8SkWX-tz3Kk2O21caE130_assertion a np:Assertion .
  dgn-np:NP86035.RAmeQMzkg67X5TS_GtJLIyunZQS8SkWX-tz3Kk2O21caE130_provenance a np:Provenance .
  dgn-np:NP86035.RAmeQMzkg67X5TS_GtJLIyunZQS8SkWX-tz3Kk2O21caE130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP86035.RAmeQMzkg67X5TS_GtJLIyunZQS8SkWX-tz3Kk2O21caE130_assertion {
  miriam-gene:348 a ncit:C16612 .
  lld:C0520679 a ncit:C7057 .
  dgn-gda:DGNf56db38aaeb1995c5a4d1b19e73b8652 sio:SIO_000628 miriam-gene:348 , lld:C0520679 ;
    a sio:SIO_001122 .
}
dgn-np:NP86035.RAmeQMzkg67X5TS_GtJLIyunZQS8SkWX-tz3Kk2O21caE130_provenance {
  dgn-np:NP86035.RAmeQMzkg67X5TS_GtJLIyunZQS8SkWX-tz3Kk2O21caE130_assertion dcterms:description "[APOE epsilon4 allele is more frequent in children with obstructive sleep apnea and particularly in those who develop neurocognitive deficits, suggesting that the APOE epsilon4 allele is associated with not only increased odds of having sleep-disordered breathing, but also with an increased risk for neurocognitive dysfunction.]. 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:17636061 ;
    prov:wasDerivedFrom dgn-void:gad-20130706 ;
    prov:wasGeneratedBy eco:ECO_0000203 .
  dgn-void:gad-20130706 pav:importedOn "2013-07-06"^^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:NP86035.RAmeQMzkg67X5TS_GtJLIyunZQS8SkWX-tz3Kk2O21caE130_publicationInfo {
  this: dcterms:created "2014-10-02T12:32:42+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" .
}