@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP182679.RAMz3pjuD263RI0JwrrQO0hvaFBS898B-QkLzJTXPmJ3Y> .
@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:NP182679.RAMz3pjuD263RI0JwrrQO0hvaFBS898B-QkLzJTXPmJ3Y130_head {
  this: np:hasAssertion dgn-np:NP182679.RAMz3pjuD263RI0JwrrQO0hvaFBS898B-QkLzJTXPmJ3Y130_assertion;
    np:hasProvenance dgn-np:NP182679.RAMz3pjuD263RI0JwrrQO0hvaFBS898B-QkLzJTXPmJ3Y130_provenance;
    np:hasPublicationInfo dgn-np:NP182679.RAMz3pjuD263RI0JwrrQO0hvaFBS898B-QkLzJTXPmJ3Y130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP182679.RAMz3pjuD263RI0JwrrQO0hvaFBS898B-QkLzJTXPmJ3Y130_assertion a np:Assertion .
  
  dgn-np:NP182679.RAMz3pjuD263RI0JwrrQO0hvaFBS898B-QkLzJTXPmJ3Y130_provenance a np:Provenance .
  
  dgn-np:NP182679.RAMz3pjuD263RI0JwrrQO0hvaFBS898B-QkLzJTXPmJ3Y130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP182679.RAMz3pjuD263RI0JwrrQO0hvaFBS898B-QkLzJTXPmJ3Y130_assertion {
  miriam-gene:341 a ncit:C16612 .
  
  lld:C0002395 a ncit:C7057 .
  
  dgn-gda:DGN3a279ff92104c4e6627d0ed15d3a4a50 sio:SIO_000628 miriam-gene:341, lld:C0002395;
    a sio:SIO_001121 .
}

dgn-np:NP182679.RAMz3pjuD263RI0JwrrQO0hvaFBS898B-QkLzJTXPmJ3Y130_provenance {
  dgn-np:NP182679.RAMz3pjuD263RI0JwrrQO0hvaFBS898B-QkLzJTXPmJ3Y130_assertion dcterms:description
      "[To identify clinical manifestations and neuropsychological effects of Alzheimer disease (AD) in apolipoprotein (ApoE) e4 carriers and to investigate the relationships between ApoE HhaI polymorphism and apolipoprotein C1 (APOC1) HpaI polymorphism in Taiwanese patients with AD.]. 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:20145290;
    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:NP182679.RAMz3pjuD263RI0JwrrQO0hvaFBS898B-QkLzJTXPmJ3Y130_publicationInfo {
  this: dcterms:created "2014-10-02T12:33:39+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" .
}