@prefix this: <http://rdf.disgenet.org/resource/nanopub/NP328091.RAx8fTnCbPQuZgIvh4aehouAoPdBOTm1DJCDCRRg0QR1M> .
@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:NP328091.RAx8fTnCbPQuZgIvh4aehouAoPdBOTm1DJCDCRRg0QR1M130_head {
  this: np:hasAssertion dgn-np:NP328091.RAx8fTnCbPQuZgIvh4aehouAoPdBOTm1DJCDCRRg0QR1M130_assertion ;
    np:hasProvenance dgn-np:NP328091.RAx8fTnCbPQuZgIvh4aehouAoPdBOTm1DJCDCRRg0QR1M130_provenance ;
    np:hasPublicationInfo dgn-np:NP328091.RAx8fTnCbPQuZgIvh4aehouAoPdBOTm1DJCDCRRg0QR1M130_publicationInfo ;
    a np:Nanopublication .
  dgn-np:NP328091.RAx8fTnCbPQuZgIvh4aehouAoPdBOTm1DJCDCRRg0QR1M130_assertion a np:Assertion .
  dgn-np:NP328091.RAx8fTnCbPQuZgIvh4aehouAoPdBOTm1DJCDCRRg0QR1M130_provenance a np:Provenance .
  dgn-np:NP328091.RAx8fTnCbPQuZgIvh4aehouAoPdBOTm1DJCDCRRg0QR1M130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP328091.RAx8fTnCbPQuZgIvh4aehouAoPdBOTm1DJCDCRRg0QR1M130_assertion {
  miriam-gene:4137 a ncit:C16612 .
  lld:C0236642 a ncit:C7057 .
  dgn-gda:DGNaeb3b301f605b0d63d45e63be8bc5fcf sio:SIO_000628 miriam-gene:4137 , lld:C0236642 ;
    a sio:SIO_001121 .
}
dgn-np:NP328091.RAx8fTnCbPQuZgIvh4aehouAoPdBOTm1DJCDCRRg0QR1M130_provenance {
  dgn-np:NP328091.RAx8fTnCbPQuZgIvh4aehouAoPdBOTm1DJCDCRRg0QR1M130_assertion dcterms:description "[Prominent filamentous tau inclusions and brain degeneration in the absence of beta-amyloid deposits are also hallmarks of neurodegenerative tauopathies exemplified by sporadic corticobasal degeneration, progressive supranuclear palsy, and Pick's disease, as well as by hereditary frontotemporal dementia and parkinsonism linked to chromosome 17 (FTDP-17).]. 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:11520930 ;
    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:NP328091.RAx8fTnCbPQuZgIvh4aehouAoPdBOTm1DJCDCRRg0QR1M130_publicationInfo {
  this: dcterms:created "2016-05-13T12:44:14+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" .
}