@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP180506.RAqmJav5wP2rDBTTj47DPm16Uv_nj_-bpFa2dg4rFnCZY> .
@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:NP180506.RAqmJav5wP2rDBTTj47DPm16Uv_nj_-bpFa2dg4rFnCZY130_head {
  this: np:hasAssertion dgn-np:NP180506.RAqmJav5wP2rDBTTj47DPm16Uv_nj_-bpFa2dg4rFnCZY130_assertion;
    np:hasProvenance dgn-np:NP180506.RAqmJav5wP2rDBTTj47DPm16Uv_nj_-bpFa2dg4rFnCZY130_provenance;
    np:hasPublicationInfo dgn-np:NP180506.RAqmJav5wP2rDBTTj47DPm16Uv_nj_-bpFa2dg4rFnCZY130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP180506.RAqmJav5wP2rDBTTj47DPm16Uv_nj_-bpFa2dg4rFnCZY130_assertion a np:Assertion .
  
  dgn-np:NP180506.RAqmJav5wP2rDBTTj47DPm16Uv_nj_-bpFa2dg4rFnCZY130_provenance a np:Provenance .
  
  dgn-np:NP180506.RAqmJav5wP2rDBTTj47DPm16Uv_nj_-bpFa2dg4rFnCZY130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP180506.RAqmJav5wP2rDBTTj47DPm16Uv_nj_-bpFa2dg4rFnCZY130_assertion {
  miriam-gene:348 a ncit:C16612 .
  
  lld:C1270972 a ncit:C7057 .
  
  dgn-gda:DGNd9484628fad8825363c95088ca80f6f0 sio:SIO_000628 miriam-gene:348, lld:C1270972;
    a sio:SIO_001121 .
}

dgn-np:NP180506.RAqmJav5wP2rDBTTj47DPm16Uv_nj_-bpFa2dg4rFnCZY130_provenance {
  dgn-np:NP180506.RAqmJav5wP2rDBTTj47DPm16Uv_nj_-bpFa2dg4rFnCZY130_assertion dcterms:description
      "[To clarify further the relationship between ApoE alleles polymorphism and cerebrovascular disease (CVD) in demented and cognitively impaired patients, we examined the ApoE phenotypes in a sample of 280 patients: 155 with AD, 21 with VaD, 32 with mixed dementia (MD), 45 with mild cognitive impairment (MCI) but without CVD, and 27 in which vascular disease was the most probable cause of cognitive decline [vascular mild cognitive impairment (VMCI)].]. 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:10362893;
    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:NP180506.RAqmJav5wP2rDBTTj47DPm16Uv_nj_-bpFa2dg4rFnCZY130_publicationInfo {
  this: dcterms:created "2014-10-02T12:33:37+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" .
}