@prefix this: <http://rdf.disgenet.org/resource/nanopub/NP1081081.RAeiloVyQ2D383v4PGdKEIpLlR6jQ3Rcbw8CB__MxSomw> .
@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/> .
@prefix wi: <http://purl.org/ontology/wi/core#> .
@prefix prov: <http://www.w3.org/ns/prov#> .
@prefix pav: <http://purl.org/pav/> .
@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/resource/nanopub/> .
@prefix dgn-gda: <http://rdf.disgenet.org/resource/gda/> .
@prefix dgn-void: <http://rdf.disgenet.org/v4.0.0/void/> .
dgn-np:NP1081081.RAeiloVyQ2D383v4PGdKEIpLlR6jQ3Rcbw8CB__MxSomw130_head {
  this: np:hasAssertion dgn-np:NP1081081.RAeiloVyQ2D383v4PGdKEIpLlR6jQ3Rcbw8CB__MxSomw130_assertion ;
    np:hasProvenance dgn-np:NP1081081.RAeiloVyQ2D383v4PGdKEIpLlR6jQ3Rcbw8CB__MxSomw130_provenance ;
    np:hasPublicationInfo dgn-np:NP1081081.RAeiloVyQ2D383v4PGdKEIpLlR6jQ3Rcbw8CB__MxSomw130_publicationInfo ;
    a np:Nanopublication .
  dgn-np:NP1081081.RAeiloVyQ2D383v4PGdKEIpLlR6jQ3Rcbw8CB__MxSomw130_assertion a np:Assertion .
  dgn-np:NP1081081.RAeiloVyQ2D383v4PGdKEIpLlR6jQ3Rcbw8CB__MxSomw130_provenance a np:Provenance .
  dgn-np:NP1081081.RAeiloVyQ2D383v4PGdKEIpLlR6jQ3Rcbw8CB__MxSomw130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP1081081.RAeiloVyQ2D383v4PGdKEIpLlR6jQ3Rcbw8CB__MxSomw130_assertion {
  miriam-gene:348 a ncit:C16612 .
  lld:C0338656 a ncit:C7057 .
  dgn-gda:DGNbaceb22db6652411eafde591c6801824 sio:SIO_000628 miriam-gene:348 , lld:C0338656 ;
    a sio:SIO_001121 .
}
dgn-np:NP1081081.RAeiloVyQ2D383v4PGdKEIpLlR6jQ3Rcbw8CB__MxSomw130_provenance {
  dgn-np:NP1081081.RAeiloVyQ2D383v4PGdKEIpLlR6jQ3Rcbw8CB__MxSomw130_assertion dcterms:description "[Although samples enriched for APOE ε4 carriers in AD or MCI clinical trials showed slightly more cognitive impairment and greater decline using the number APOE ε4 alleles as an inclusion criterion most likely would not result in more efficient trials, and trials would take longer because fewer patients would be available.]. 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:23712001 ;
    prov:wasDerivedFrom dgn-void:befree-2016 ;
    prov:wasGeneratedBy eco:ECO_0000203 .
  dgn-void:befree-2016 pav:importedOn "2016-02-19"^^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:NP1081081.RAeiloVyQ2D383v4PGdKEIpLlR6jQ3Rcbw8CB__MxSomw130_publicationInfo {
  this: dcterms:created "2016-05-13T12:49:56+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:disgenetv3.0rdf ;
    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 "v4.0.0.0" .
  dgn-void:disgenetv3.0rdf pav:version "v4.0.0" .
}