@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP721379.RAD0Urf6-936t4NIx3723iD0OEwpRAGr4daKzW3JXI_NU> .
@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:NP721379.RAD0Urf6-936t4NIx3723iD0OEwpRAGr4daKzW3JXI_NU130_head {
  this: np:hasAssertion dgn-np:NP721379.RAD0Urf6-936t4NIx3723iD0OEwpRAGr4daKzW3JXI_NU130_assertion ;
    np:hasProvenance dgn-np:NP721379.RAD0Urf6-936t4NIx3723iD0OEwpRAGr4daKzW3JXI_NU130_provenance ;
    np:hasPublicationInfo dgn-np:NP721379.RAD0Urf6-936t4NIx3723iD0OEwpRAGr4daKzW3JXI_NU130_publicationInfo ;
    a np:Nanopublication .
  dgn-np:NP721379.RAD0Urf6-936t4NIx3723iD0OEwpRAGr4daKzW3JXI_NU130_assertion a np:Assertion .
  dgn-np:NP721379.RAD0Urf6-936t4NIx3723iD0OEwpRAGr4daKzW3JXI_NU130_provenance a np:Provenance .
  dgn-np:NP721379.RAD0Urf6-936t4NIx3723iD0OEwpRAGr4daKzW3JXI_NU130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP721379.RAD0Urf6-936t4NIx3723iD0OEwpRAGr4daKzW3JXI_NU130_assertion {
  miriam-gene:348 a ncit:C16612 .
  lld:C0241970 a ncit:C7057 .
  dgn-gda:DGN1d30fbe501828b98cd45a8312f23508b sio:SIO_000628 miriam-gene:348 , lld:C0241970 ;
    a sio:SIO_001121 .
}
dgn-np:NP721379.RAD0Urf6-936t4NIx3723iD0OEwpRAGr4daKzW3JXI_NU130_provenance {
  dgn-np:NP721379.RAD0Urf6-936t4NIx3723iD0OEwpRAGr4daKzW3JXI_NU130_assertion dcterms:description "[When neuropsychological measures were included in the analysis, memory (HR = 0.90 [95% CI 0.84 to 0.96], p = 0.002) and executive function (HR = 0.96 [95% CI 0.92 to 1.0], p = 0.045) were associated with increased risk of dementia progression, whereas APOE genotype, cerebrovascular risk factors, clinical stroke, presence or absence of lacunes, and extent of white matter hyperintensities did not predict progression.]. 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:15277612 ;
    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:NP721379.RAD0Urf6-936t4NIx3723iD0OEwpRAGr4daKzW3JXI_NU130_publicationInfo {
  this: dcterms:created "2014-10-02T12:39:18+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" .
}