@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP787792.RAhrqsQzHGBZSM0ocWJxQ6a1TY47EIqRZWWsJGpObX65I> .
@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:NP787792.RAhrqsQzHGBZSM0ocWJxQ6a1TY47EIqRZWWsJGpObX65I130_head {
  this: np:hasAssertion dgn-np:NP787792.RAhrqsQzHGBZSM0ocWJxQ6a1TY47EIqRZWWsJGpObX65I130_assertion ;
    np:hasProvenance dgn-np:NP787792.RAhrqsQzHGBZSM0ocWJxQ6a1TY47EIqRZWWsJGpObX65I130_provenance ;
    np:hasPublicationInfo dgn-np:NP787792.RAhrqsQzHGBZSM0ocWJxQ6a1TY47EIqRZWWsJGpObX65I130_publicationInfo ;
    a np:Nanopublication .
  dgn-np:NP787792.RAhrqsQzHGBZSM0ocWJxQ6a1TY47EIqRZWWsJGpObX65I130_assertion a np:Assertion .
  dgn-np:NP787792.RAhrqsQzHGBZSM0ocWJxQ6a1TY47EIqRZWWsJGpObX65I130_provenance a np:Provenance .
  dgn-np:NP787792.RAhrqsQzHGBZSM0ocWJxQ6a1TY47EIqRZWWsJGpObX65I130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP787792.RAhrqsQzHGBZSM0ocWJxQ6a1TY47EIqRZWWsJGpObX65I130_assertion {
  miriam-gene:348 a ncit:C16612 .
  lld:C0007787 a ncit:C7057 .
  dgn-gda:DGN6953e19170d19e3297e65e70ed6dc0dc sio:SIO_000628 miriam-gene:348 , lld:C0007787 ;
    a sio:SIO_001121 .
}
dgn-np:NP787792.RAhrqsQzHGBZSM0ocWJxQ6a1TY47EIqRZWWsJGpObX65I130_provenance {
  dgn-np:NP787792.RAhrqsQzHGBZSM0ocWJxQ6a1TY47EIqRZWWsJGpObX65I130_assertion dcterms:description "[To investigate whether the APOE*4 allele modified the relationship between cerebrovascular events and Alzheimer's disease (AD), we collected evidence of previous stroke or transient ischemic attack (TIA) and determined APOE genotype among 102 subjects with AD and 375 nondemented subjects in a community-based study of dementia.]. 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:11060506 ;
    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:NP787792.RAhrqsQzHGBZSM0ocWJxQ6a1TY47EIqRZWWsJGpObX65I130_publicationInfo {
  this: dcterms:created "2014-10-02T12:40:00+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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}