@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP217004.RAdkE0KEOcHLXccQpC-fEte-pG70_mKPTf6MtJqMyQeug> .
@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:NP217004.RAdkE0KEOcHLXccQpC-fEte-pG70_mKPTf6MtJqMyQeug130_head {
  this: np:hasAssertion dgn-np:NP217004.RAdkE0KEOcHLXccQpC-fEte-pG70_mKPTf6MtJqMyQeug130_assertion ;
    np:hasProvenance dgn-np:NP217004.RAdkE0KEOcHLXccQpC-fEte-pG70_mKPTf6MtJqMyQeug130_provenance ;
    np:hasPublicationInfo dgn-np:NP217004.RAdkE0KEOcHLXccQpC-fEte-pG70_mKPTf6MtJqMyQeug130_publicationInfo ;
    a np:Nanopublication .
  dgn-np:NP217004.RAdkE0KEOcHLXccQpC-fEte-pG70_mKPTf6MtJqMyQeug130_assertion a np:Assertion .
  dgn-np:NP217004.RAdkE0KEOcHLXccQpC-fEte-pG70_mKPTf6MtJqMyQeug130_provenance a np:Provenance .
  dgn-np:NP217004.RAdkE0KEOcHLXccQpC-fEte-pG70_mKPTf6MtJqMyQeug130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP217004.RAdkE0KEOcHLXccQpC-fEte-pG70_mKPTf6MtJqMyQeug130_assertion {
  miriam-gene:3630 a ncit:C16612 .
  lld:C0338656 a ncit:C7057 .
  dgn-gda:DGNc7093c44aa433ec70cc714a3ba8b5c6e sio:SIO_000628 miriam-gene:3630 , lld:C0338656 ;
    a sio:SIO_001121 .
}
dgn-np:NP217004.RAdkE0KEOcHLXccQpC-fEte-pG70_mKPTf6MtJqMyQeug130_provenance {
  dgn-np:NP217004.RAdkE0KEOcHLXccQpC-fEte-pG70_mKPTf6MtJqMyQeug130_assertion dcterms:description "[The subgroup showing neither a CVD pattern nor an AD pattern had significantly older age, higher hemoglobin A1c level, longer duration of diabetes, higher frequency of insulin therapy, lower frequency of apolipoprotein E4 carriers, less severe medial temporal lobe atrophy, more impaired attention, less impaired word recall, and slower progression of cognitive impairment than the subgroup showing an AD pattern.]. 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:23594859 ;
    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:NP217004.RAdkE0KEOcHLXccQpC-fEte-pG70_mKPTf6MtJqMyQeug130_publicationInfo {
  this: dcterms:created "2014-10-02T12:34:00+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" .
  dgn-void:disgenetrdf pav:version "v2.1.0" .
}