@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP48257.RAAsoPrxxyzxBX_VhI6Yn5_-5V4W44mpNgcKjlNT8tmUI> .
@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:NP48257.RAAsoPrxxyzxBX_VhI6Yn5_-5V4W44mpNgcKjlNT8tmUI130_head {
  this: np:hasAssertion dgn-np:NP48257.RAAsoPrxxyzxBX_VhI6Yn5_-5V4W44mpNgcKjlNT8tmUI130_assertion;
    np:hasProvenance dgn-np:NP48257.RAAsoPrxxyzxBX_VhI6Yn5_-5V4W44mpNgcKjlNT8tmUI130_provenance;
    np:hasPublicationInfo dgn-np:NP48257.RAAsoPrxxyzxBX_VhI6Yn5_-5V4W44mpNgcKjlNT8tmUI130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP48257.RAAsoPrxxyzxBX_VhI6Yn5_-5V4W44mpNgcKjlNT8tmUI130_assertion a np:Assertion .
  
  dgn-np:NP48257.RAAsoPrxxyzxBX_VhI6Yn5_-5V4W44mpNgcKjlNT8tmUI130_provenance a np:Provenance .
  
  dgn-np:NP48257.RAAsoPrxxyzxBX_VhI6Yn5_-5V4W44mpNgcKjlNT8tmUI130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP48257.RAAsoPrxxyzxBX_VhI6Yn5_-5V4W44mpNgcKjlNT8tmUI130_assertion {
  miriam-gene:348 a ncit:C16612 .
  
  lld:C0007820 a ncit:C7057 .
  
  dgn-gda:DGN33759efa1819460167b000e1973331d1 sio:SIO_000628 miriam-gene:348, lld:C0007820;
    a sio:SIO_001122 .
}

dgn-np:NP48257.RAAsoPrxxyzxBX_VhI6Yn5_-5V4W44mpNgcKjlNT8tmUI130_provenance {
  dgn-np:NP48257.RAAsoPrxxyzxBX_VhI6Yn5_-5V4W44mpNgcKjlNT8tmUI130_assertion dcterms:description
      "[The apoE4 allele exacerbates the effects of cerebrovascular risk factors on NP function. This relationship appears to be driven by SBP, suggesting that treatment of high SBP could potentially reduce risk of cognitive impairment among those already at increased risk for Alzheimer disease.]. 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:20471857;
    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:NP48257.RAAsoPrxxyzxBX_VhI6Yn5_-5V4W44mpNgcKjlNT8tmUI130_publicationInfo {
  this: dcterms:created "2014-10-02T12:32:22+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" .
}