@prefix this: <http://rdf.disgenet.org/resource/nanopub/NP373131.RAtO00s9XYfxg4UaTrMxi02GQDrIn__4kfDmUvZnO9FmU> .
@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/> .
@prefix wi: <http://purl.org/ontology/wi/core#> .
@prefix prov: <http://www.w3.org/ns/prov#> .
@prefix pav: <http://purl.org/pav/> .
@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/resource/nanopub/> .
@prefix dgn-gda: <http://rdf.disgenet.org/resource/gda/> .
@prefix dgn-void: <http://rdf.disgenet.org/v4.0.0/void/> .

dgn-np:NP373131.RAtO00s9XYfxg4UaTrMxi02GQDrIn__4kfDmUvZnO9FmU130_head {
  this: np:hasAssertion dgn-np:NP373131.RAtO00s9XYfxg4UaTrMxi02GQDrIn__4kfDmUvZnO9FmU130_assertion;
    np:hasProvenance dgn-np:NP373131.RAtO00s9XYfxg4UaTrMxi02GQDrIn__4kfDmUvZnO9FmU130_provenance;
    np:hasPublicationInfo dgn-np:NP373131.RAtO00s9XYfxg4UaTrMxi02GQDrIn__4kfDmUvZnO9FmU130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP373131.RAtO00s9XYfxg4UaTrMxi02GQDrIn__4kfDmUvZnO9FmU130_assertion a np:Assertion .
  
  dgn-np:NP373131.RAtO00s9XYfxg4UaTrMxi02GQDrIn__4kfDmUvZnO9FmU130_provenance a np:Provenance .
  
  dgn-np:NP373131.RAtO00s9XYfxg4UaTrMxi02GQDrIn__4kfDmUvZnO9FmU130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP373131.RAtO00s9XYfxg4UaTrMxi02GQDrIn__4kfDmUvZnO9FmU130_assertion {
  miriam-gene:4137 a ncit:C16612 .
  
  lld:C0333463 a ncit:C7057 .
  
  dgn-gda:DGN03fdeadea935f41f85391e1e9b2e6e2a sio:SIO_000628 miriam-gene:4137, lld:C0333463;
    a sio:SIO_001122 .
}

dgn-np:NP373131.RAtO00s9XYfxg4UaTrMxi02GQDrIn__4kfDmUvZnO9FmU130_provenance {
  dgn-np:NP373131.RAtO00s9XYfxg4UaTrMxi02GQDrIn__4kfDmUvZnO9FmU130_assertion dcterms:description
      "[These findings suggest that (1) LB pathology can influence the clinical features of familial AD, (2) the E184D mutation of presenilin-1 may be associated with the LB formation through Abeta overproduction, although the process of LB formation is strongly affected by other unknown mechanisms, (3) in neurodegenerative disorders with LBs, there is a common pathophysiological background inducing NAC accumulation in neuritic plaques and astrocytes, and (4) the NAC accumulation in neuritic plaques is modulated by the abnormally aggregated tau protein.]. 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:12410385;
    prov:wasDerivedFrom dgn-void:befree-2016;
    prov:wasGeneratedBy eco:ECO_0000203 .
  
  dgn-void:befree-2016 pav:importedOn "2016-02-19"^^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:NP373131.RAtO00s9XYfxg4UaTrMxi02GQDrIn__4kfDmUvZnO9FmU130_publicationInfo {
  this: dcterms:created "2016-05-13T12:44:34+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:disgenetv3.0rdf;
    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 "v4.0.0.0" .
  
  dgn-void:disgenetv3.0rdf pav:version "v4.0.0" .
}