@prefix this: <http://rdf.disgenet.org/resource/nanopub/NP940376.RAsJApW_4E-DNr7S9zOndagOKJElIfWuMQta1oxQS8NB8> .
@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:NP940376.RAsJApW_4E-DNr7S9zOndagOKJElIfWuMQta1oxQS8NB8130_head {
  this: np:hasAssertion dgn-np:NP940376.RAsJApW_4E-DNr7S9zOndagOKJElIfWuMQta1oxQS8NB8130_assertion ;
    np:hasProvenance dgn-np:NP940376.RAsJApW_4E-DNr7S9zOndagOKJElIfWuMQta1oxQS8NB8130_provenance ;
    np:hasPublicationInfo dgn-np:NP940376.RAsJApW_4E-DNr7S9zOndagOKJElIfWuMQta1oxQS8NB8130_publicationInfo ;
    a np:Nanopublication .
  dgn-np:NP940376.RAsJApW_4E-DNr7S9zOndagOKJElIfWuMQta1oxQS8NB8130_assertion a np:Assertion .
  dgn-np:NP940376.RAsJApW_4E-DNr7S9zOndagOKJElIfWuMQta1oxQS8NB8130_provenance a np:Provenance .
  dgn-np:NP940376.RAsJApW_4E-DNr7S9zOndagOKJElIfWuMQta1oxQS8NB8130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP940376.RAsJApW_4E-DNr7S9zOndagOKJElIfWuMQta1oxQS8NB8130_assertion {
  miriam-gene:4137 a ncit:C16612 .
  lld:C0236642 a ncit:C7057 .
  dgn-gda:DGN24244b52621049d871f07733852d1d58 sio:SIO_000628 miriam-gene:4137 , lld:C0236642 ;
    a sio:SIO_001121 .
}
dgn-np:NP940376.RAsJApW_4E-DNr7S9zOndagOKJElIfWuMQta1oxQS8NB8130_provenance {
  dgn-np:NP940376.RAsJApW_4E-DNr7S9zOndagOKJElIfWuMQta1oxQS8NB8130_assertion dcterms:description "[The aim of the present study is to investigate UPR activation in sporadic tauopathies like progressive supranuclear palsy (PSP) and Pick's disease (PiD), and familial cases with frontotemporal dementia and parkinsonism linked to chromosome 17 (FTDP-17) which carry mutations in the gene encoding for tau (MAPT).]. 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:22102449 ;
    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:NP940376.RAsJApW_4E-DNr7S9zOndagOKJElIfWuMQta1oxQS8NB8130_publicationInfo {
  this: dcterms:created "2016-05-13T12:48:51+02:00"^^xsd:dateTime ;
    dcterms:rights <http://opendatacommons.org/licenses/odbl/1.0/> ;
    dcterms:rightsHolder dgn-void:IBIGroup ;
    dcterms:subject sio:SIO_000983 ;
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    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" .
}