@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP608936.RAfnHyYSUeSFExTOyOauXk6UI2OaQeqzqrynaeuVCfBgs> .
@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:NP608936.RAfnHyYSUeSFExTOyOauXk6UI2OaQeqzqrynaeuVCfBgs130_head {
  this: np:hasAssertion dgn-np:NP608936.RAfnHyYSUeSFExTOyOauXk6UI2OaQeqzqrynaeuVCfBgs130_assertion;
    np:hasProvenance dgn-np:NP608936.RAfnHyYSUeSFExTOyOauXk6UI2OaQeqzqrynaeuVCfBgs130_provenance;
    np:hasPublicationInfo dgn-np:NP608936.RAfnHyYSUeSFExTOyOauXk6UI2OaQeqzqrynaeuVCfBgs130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP608936.RAfnHyYSUeSFExTOyOauXk6UI2OaQeqzqrynaeuVCfBgs130_assertion a np:Assertion .
  
  dgn-np:NP608936.RAfnHyYSUeSFExTOyOauXk6UI2OaQeqzqrynaeuVCfBgs130_provenance a np:Provenance .
  
  dgn-np:NP608936.RAfnHyYSUeSFExTOyOauXk6UI2OaQeqzqrynaeuVCfBgs130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP608936.RAfnHyYSUeSFExTOyOauXk6UI2OaQeqzqrynaeuVCfBgs130_assertion {
  miriam-gene:1437 a ncit:C16612 .
  
  lld:C0085400 a ncit:C7057 .
  
  dgn-gda:DGN9cf528b9fa1320fd64ae5ec3245f27d9 sio:SIO_000628 miriam-gene:1437, lld:C0085400;
    a sio:SIO_001121 .
}

dgn-np:NP608936.RAfnHyYSUeSFExTOyOauXk6UI2OaQeqzqrynaeuVCfBgs130_provenance {
  dgn-np:NP608936.RAfnHyYSUeSFExTOyOauXk6UI2OaQeqzqrynaeuVCfBgs130_assertion dcterms:description
      "[Neuropathological studies of young deceased ε4 carriers have shown modest but abnormal amounts of neocortical amyloid and medial temporal neurofibrillary tangles that is also reflected in cerebrospinal fluid (CSF) biomarkers, amyloid-β, and phospho-tau in particular.]. 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:22695623;
    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:NP608936.RAfnHyYSUeSFExTOyOauXk6UI2OaQeqzqrynaeuVCfBgs130_publicationInfo {
  this: dcterms:created "2014-10-02T12:38:05+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" .
}