@prefix this: <http://rdf.disgenet.org/resource/nanopub/NP665036.RA7imWzN93rUBeQt7RoHAWyQfxkJPP8m6NAI5UQr5GNnU> .
@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:NP665036.RA7imWzN93rUBeQt7RoHAWyQfxkJPP8m6NAI5UQr5GNnU130_head {
   this: np:hasAssertion dgn-np:NP665036.RA7imWzN93rUBeQt7RoHAWyQfxkJPP8m6NAI5UQr5GNnU130_assertion ;
    np:hasProvenance dgn-np:NP665036.RA7imWzN93rUBeQt7RoHAWyQfxkJPP8m6NAI5UQr5GNnU130_provenance ;
    np:hasPublicationInfo dgn-np:NP665036.RA7imWzN93rUBeQt7RoHAWyQfxkJPP8m6NAI5UQr5GNnU130_publicationInfo ;
    a np:Nanopublication .
  dgn-np:NP665036.RA7imWzN93rUBeQt7RoHAWyQfxkJPP8m6NAI5UQr5GNnU130_assertion a np:Assertion .
  dgn-np:NP665036.RA7imWzN93rUBeQt7RoHAWyQfxkJPP8m6NAI5UQr5GNnU130_provenance a np:Provenance .
  dgn-np:NP665036.RA7imWzN93rUBeQt7RoHAWyQfxkJPP8m6NAI5UQr5GNnU130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP665036.RA7imWzN93rUBeQt7RoHAWyQfxkJPP8m6NAI5UQr5GNnU130_assertion {
   miriam-gene:348 a ncit:C16612 .
  lld:C0002395 a ncit:C7057 .
  dgn-gda:DGNd904edefa9bf2fb10243979e85bd4865 sio:SIO_000628 miriam-gene:348 , lld:C0002395 ;
    a sio:SIO_001121 .
}
dgn-np:NP665036.RA7imWzN93rUBeQt7RoHAWyQfxkJPP8m6NAI5UQr5GNnU130_provenance {
   dgn-np:NP665036.RA7imWzN93rUBeQt7RoHAWyQfxkJPP8m6NAI5UQr5GNnU130_assertion dcterms:description "[This finding is of great clinical importance as nondemented patients positive for APOE epsilon4 could be identified as being at genetic risk of AD, and for that reason monitored more closely.]. 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:18401171 ;
    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:NP665036.RA7imWzN93rUBeQt7RoHAWyQfxkJPP8m6NAI5UQr5GNnU130_publicationInfo {
   this: dcterms:created "2016-05-13T12:46:47+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" .
}