@prefix this: <http://rdf.disgenet.org/resource/nanopub/NP376895.RAec2lEto0bcForACIgXQsGYoZkpnQhzX5ezukDn2vZ7M> .
@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:NP376895.RAec2lEto0bcForACIgXQsGYoZkpnQhzX5ezukDn2vZ7M130_head {
  this: np:hasAssertion dgn-np:NP376895.RAec2lEto0bcForACIgXQsGYoZkpnQhzX5ezukDn2vZ7M130_assertion;
    np:hasProvenance dgn-np:NP376895.RAec2lEto0bcForACIgXQsGYoZkpnQhzX5ezukDn2vZ7M130_provenance;
    np:hasPublicationInfo dgn-np:NP376895.RAec2lEto0bcForACIgXQsGYoZkpnQhzX5ezukDn2vZ7M130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP376895.RAec2lEto0bcForACIgXQsGYoZkpnQhzX5ezukDn2vZ7M130_assertion a np:Assertion .
  
  dgn-np:NP376895.RAec2lEto0bcForACIgXQsGYoZkpnQhzX5ezukDn2vZ7M130_provenance a np:Provenance .
  
  dgn-np:NP376895.RAec2lEto0bcForACIgXQsGYoZkpnQhzX5ezukDn2vZ7M130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP376895.RAec2lEto0bcForACIgXQsGYoZkpnQhzX5ezukDn2vZ7M130_assertion {
  miriam-gene:4137 a ncit:C16612 .
  
  lld:C0242422 a ncit:C7057 .
  
  dgn-gda:DGNc86baba154d5be0595f30239f70d9e91 sio:SIO_000628 miriam-gene:4137, lld:C0242422;
    a sio:SIO_001121 .
}

dgn-np:NP376895.RAec2lEto0bcForACIgXQsGYoZkpnQhzX5ezukDn2vZ7M130_provenance {
  dgn-np:NP376895.RAec2lEto0bcForACIgXQsGYoZkpnQhzX5ezukDn2vZ7M130_assertion dcterms:description
      "[However, since 1998, the identification of more than 25 mutations in the tau gene, associated with frontotemporal dementia and parkinsonism linked to chromosome 17, has demonstrated that tau dysfunction can lead to neurodegeneration and the development of clinical symptoms.]. 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:12470988;
    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:NP376895.RAec2lEto0bcForACIgXQsGYoZkpnQhzX5ezukDn2vZ7M130_publicationInfo {
  this: dcterms:created "2016-05-13T12:44:36+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" .
}