@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP258006.RAmizlCZxZFN4wi9U205YtBoXwz9d34NDs95gILRBs2YI> .
@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:NP258006.RAmizlCZxZFN4wi9U205YtBoXwz9d34NDs95gILRBs2YI130_head {
  this: np:hasAssertion dgn-np:NP258006.RAmizlCZxZFN4wi9U205YtBoXwz9d34NDs95gILRBs2YI130_assertion;
    np:hasProvenance dgn-np:NP258006.RAmizlCZxZFN4wi9U205YtBoXwz9d34NDs95gILRBs2YI130_provenance;
    np:hasPublicationInfo dgn-np:NP258006.RAmizlCZxZFN4wi9U205YtBoXwz9d34NDs95gILRBs2YI130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP258006.RAmizlCZxZFN4wi9U205YtBoXwz9d34NDs95gILRBs2YI130_assertion a np:Assertion .
  
  dgn-np:NP258006.RAmizlCZxZFN4wi9U205YtBoXwz9d34NDs95gILRBs2YI130_provenance a np:Provenance .
  
  dgn-np:NP258006.RAmizlCZxZFN4wi9U205YtBoXwz9d34NDs95gILRBs2YI130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP258006.RAmizlCZxZFN4wi9U205YtBoXwz9d34NDs95gILRBs2YI130_assertion {
  miriam-gene:348 a ncit:C16612 .
  
  lld:C0014038 a ncit:C7057 .
  
  dgn-gda:DGN1ea83111c050ac281b3be326128ea0cf sio:SIO_000628 miriam-gene:348, lld:C0014038;
    a sio:SIO_001121 .
}

dgn-np:NP258006.RAmizlCZxZFN4wi9U205YtBoXwz9d34NDs95gILRBs2YI130_provenance {
  dgn-np:NP258006.RAmizlCZxZFN4wi9U205YtBoXwz9d34NDs95gILRBs2YI130_assertion dcterms:description
      "[Herein, we have expanded the study group to 19 AD patients homozygous for APOE4 or APOE3, as well as 30 patients with other neurodegenerative diseases, including diffuse Lewy body disease, Pick's disease, progressive supranuclear palsy, Parkinson's disease, and human immunodeficiency virus-1 encephalitis.]. 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:9258256;
    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:NP258006.RAmizlCZxZFN4wi9U205YtBoXwz9d34NDs95gILRBs2YI130_publicationInfo {
  this: dcterms:created "2014-10-02T12:34:24+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" .
}