@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP934376.RAtcc5BQtFg98OyR0KQvu9QGX7mALnMtwkVqbtXGRi724> .
@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:NP934376.RAtcc5BQtFg98OyR0KQvu9QGX7mALnMtwkVqbtXGRi724130_head {
   this: np:hasAssertion dgn-np:NP934376.RAtcc5BQtFg98OyR0KQvu9QGX7mALnMtwkVqbtXGRi724130_assertion ;
    np:hasProvenance dgn-np:NP934376.RAtcc5BQtFg98OyR0KQvu9QGX7mALnMtwkVqbtXGRi724130_provenance ;
    np:hasPublicationInfo dgn-np:NP934376.RAtcc5BQtFg98OyR0KQvu9QGX7mALnMtwkVqbtXGRi724130_publicationInfo ;
    a np:Nanopublication .
  dgn-np:NP934376.RAtcc5BQtFg98OyR0KQvu9QGX7mALnMtwkVqbtXGRi724130_assertion a np:Assertion .
  dgn-np:NP934376.RAtcc5BQtFg98OyR0KQvu9QGX7mALnMtwkVqbtXGRi724130_provenance a np:Provenance .
  dgn-np:NP934376.RAtcc5BQtFg98OyR0KQvu9QGX7mALnMtwkVqbtXGRi724130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP934376.RAtcc5BQtFg98OyR0KQvu9QGX7mALnMtwkVqbtXGRi724130_assertion {
   miriam-gene:348 a ncit:C16612 .
  lld:C0011854 a ncit:C7057 .
  dgn-gda:DGNb8bedd8d66c8ac3b167bdd69a57e5199 sio:SIO_000628 miriam-gene:348 , lld:C0011854 ;
    a sio:SIO_001121 .
}
dgn-np:NP934376.RAtcc5BQtFg98OyR0KQvu9QGX7mALnMtwkVqbtXGRi724130_provenance {
   dgn-np:NP934376.RAtcc5BQtFg98OyR0KQvu9QGX7mALnMtwkVqbtXGRi724130_assertion dcterms:description "[Specific polymorphisms of the apolipoprotein E (APOE) and angiotensin-converting enzyme (ACE) genes appear to increase risk for Alzheimer's disease and cognitive dysfunction in the general population, yet little research has examined whether genetic factors influence risk of cognitive dysfunction in patients with Type 1 diabetes.]. 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:20121884 ;
    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:NP934376.RAtcc5BQtFg98OyR0KQvu9QGX7mALnMtwkVqbtXGRi724130_publicationInfo {
   this: dcterms:created "2014-10-02T12:41:32+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" .
}