@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP154679.RAYTc4ynK7EaiPxI5vWBPsvREd87mUsy1tHtDN2abxkRI> .
@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:NP154679.RAYTc4ynK7EaiPxI5vWBPsvREd87mUsy1tHtDN2abxkRI130_head {
  this: np:hasAssertion dgn-np:NP154679.RAYTc4ynK7EaiPxI5vWBPsvREd87mUsy1tHtDN2abxkRI130_assertion;
    np:hasProvenance dgn-np:NP154679.RAYTc4ynK7EaiPxI5vWBPsvREd87mUsy1tHtDN2abxkRI130_provenance;
    np:hasPublicationInfo dgn-np:NP154679.RAYTc4ynK7EaiPxI5vWBPsvREd87mUsy1tHtDN2abxkRI130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP154679.RAYTc4ynK7EaiPxI5vWBPsvREd87mUsy1tHtDN2abxkRI130_assertion a np:Assertion .
  
  dgn-np:NP154679.RAYTc4ynK7EaiPxI5vWBPsvREd87mUsy1tHtDN2abxkRI130_provenance a np:Provenance .
  
  dgn-np:NP154679.RAYTc4ynK7EaiPxI5vWBPsvREd87mUsy1tHtDN2abxkRI130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP154679.RAYTc4ynK7EaiPxI5vWBPsvREd87mUsy1tHtDN2abxkRI130_assertion {
  miriam-gene:348 a ncit:C16612 .
  
  lld:C0002395 a ncit:C7057 .
  
  dgn-gda:DGNb7328984d6835ce351ba796e927728db sio:SIO_000628 miriam-gene:348, lld:C0002395;
    a sio:SIO_001121 .
}

dgn-np:NP154679.RAYTc4ynK7EaiPxI5vWBPsvREd87mUsy1tHtDN2abxkRI130_provenance {
  dgn-np:NP154679.RAYTc4ynK7EaiPxI5vWBPsvREd87mUsy1tHtDN2abxkRI130_assertion dcterms:description
      "[Assessment of sleep consolidation may identify APOE+ individuals at high risk for incident AD, and interventions to enhance sleep consolidation should be studied as potentially useful means to reduce the risk of AD and development of neurofibrillary tangles in APOE ε4+ individuals.]. 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:24145819;
    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:NP154679.RAYTc4ynK7EaiPxI5vWBPsvREd87mUsy1tHtDN2abxkRI130_publicationInfo {
  this: dcterms:created "2014-10-02T12:33:22+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" .
}