@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP282599.RAsLyl5ODHYBcNcbjVDFxC6fm4Tl4_KGqs_kJRj4zk1FA> .
@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:NP282599.RAsLyl5ODHYBcNcbjVDFxC6fm4Tl4_KGqs_kJRj4zk1FA130_head {
  this: np:hasAssertion dgn-np:NP282599.RAsLyl5ODHYBcNcbjVDFxC6fm4Tl4_KGqs_kJRj4zk1FA130_assertion ;
    np:hasProvenance dgn-np:NP282599.RAsLyl5ODHYBcNcbjVDFxC6fm4Tl4_KGqs_kJRj4zk1FA130_provenance ;
    np:hasPublicationInfo dgn-np:NP282599.RAsLyl5ODHYBcNcbjVDFxC6fm4Tl4_KGqs_kJRj4zk1FA130_publicationInfo ;
    a np:Nanopublication .
  dgn-np:NP282599.RAsLyl5ODHYBcNcbjVDFxC6fm4Tl4_KGqs_kJRj4zk1FA130_assertion a np:Assertion .
  dgn-np:NP282599.RAsLyl5ODHYBcNcbjVDFxC6fm4Tl4_KGqs_kJRj4zk1FA130_provenance a np:Provenance .
  dgn-np:NP282599.RAsLyl5ODHYBcNcbjVDFxC6fm4Tl4_KGqs_kJRj4zk1FA130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP282599.RAsLyl5ODHYBcNcbjVDFxC6fm4Tl4_KGqs_kJRj4zk1FA130_assertion {
  miriam-gene:1378 a ncit:C16612 .
  lld:C0002395 a ncit:C7057 .
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    a sio:SIO_001121 .
}
dgn-np:NP282599.RAsLyl5ODHYBcNcbjVDFxC6fm4Tl4_KGqs_kJRj4zk1FA130_provenance {
  dgn-np:NP282599.RAsLyl5ODHYBcNcbjVDFxC6fm4Tl4_KGqs_kJRj4zk1FA130_assertion dcterms:description "[Genetic variations in CLU, PICALM, and CR1 are associated with Alzheimer's disease, but it is unknown whether they exert their effects by altering cognitive trajectory in elderly individuals at risk for the 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:22952074 ;
    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:NP282599.RAsLyl5ODHYBcNcbjVDFxC6fm4Tl4_KGqs_kJRj4zk1FA130_publicationInfo {
  this: dcterms:created "2014-10-02T12:34:39+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" .
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}