@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP258467.RAoXLn-vSESF1TE5UAgue2nClNC6PQOAeF8MWPZZY5djo> .
@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:NP258467.RAoXLn-vSESF1TE5UAgue2nClNC6PQOAeF8MWPZZY5djo130_head {
  this: np:hasAssertion dgn-np:NP258467.RAoXLn-vSESF1TE5UAgue2nClNC6PQOAeF8MWPZZY5djo130_assertion;
    np:hasProvenance dgn-np:NP258467.RAoXLn-vSESF1TE5UAgue2nClNC6PQOAeF8MWPZZY5djo130_provenance;
    np:hasPublicationInfo dgn-np:NP258467.RAoXLn-vSESF1TE5UAgue2nClNC6PQOAeF8MWPZZY5djo130_publicationInfo;
    a np:Nanopublication .
  
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dgn-np:NP258467.RAoXLn-vSESF1TE5UAgue2nClNC6PQOAeF8MWPZZY5djo130_assertion {
  miriam-gene:348 a ncit:C16612 .
  
  lld:C1270972 a ncit:C7057 .
  
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dgn-np:NP258467.RAoXLn-vSESF1TE5UAgue2nClNC6PQOAeF8MWPZZY5djo130_provenance {
  dgn-np:NP258467.RAoXLn-vSESF1TE5UAgue2nClNC6PQOAeF8MWPZZY5djo130_assertion dcterms:description
      "[We examined the improvement in statistical power that could be obtained in therapeutic trials for early (predementia) Alzheimer disease by constraining enrollment to individuals with amnestic mild cognitive impairment (MCI) and an atrophy pattern on a screening magnetic resonance imaging (MRI) scan previously found to be predictive of clinical decline, or to individuals with MCI and the apolipoprotein E epsilon 4 genetic risk factor 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;
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    prov:wasDerivedFrom dgn-void:befree-20140225;
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  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 .
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dgn-np:NP258467.RAoXLn-vSESF1TE5UAgue2nClNC6PQOAeF8MWPZZY5djo130_publicationInfo {
  this: dcterms:created "2014-10-02T12:34:24+02:00"^^xsd:dateTime;
    dcterms:rights <http://opendatacommons.org/licenses/odbl/1.0/>;
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    dcterms:subject sio:SIO_000983;
    prv:usedData dgn-void:disgenetrdf;
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    pav:version "v2.1.0.0" .
  
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