@prefix this: <http://rdf.disgenet.org/resource/nanopub/NP940378.RAiEj_EGIe9Cyct8l5fNwH__c8Yi4L31jOSQoFhua3w4Q> .
@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:NP940378.RAiEj_EGIe9Cyct8l5fNwH__c8Yi4L31jOSQoFhua3w4Q130_head {
  this: np:hasAssertion dgn-np:NP940378.RAiEj_EGIe9Cyct8l5fNwH__c8Yi4L31jOSQoFhua3w4Q130_assertion;
    np:hasProvenance dgn-np:NP940378.RAiEj_EGIe9Cyct8l5fNwH__c8Yi4L31jOSQoFhua3w4Q130_provenance;
    np:hasPublicationInfo dgn-np:NP940378.RAiEj_EGIe9Cyct8l5fNwH__c8Yi4L31jOSQoFhua3w4Q130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP940378.RAiEj_EGIe9Cyct8l5fNwH__c8Yi4L31jOSQoFhua3w4Q130_assertion a np:Assertion .
  
  dgn-np:NP940378.RAiEj_EGIe9Cyct8l5fNwH__c8Yi4L31jOSQoFhua3w4Q130_provenance a np:Provenance .
  
  dgn-np:NP940378.RAiEj_EGIe9Cyct8l5fNwH__c8Yi4L31jOSQoFhua3w4Q130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP940378.RAiEj_EGIe9Cyct8l5fNwH__c8Yi4L31jOSQoFhua3w4Q130_assertion {
  miriam-gene:4137 a ncit:C16612 .
  
  lld:C0949664 a ncit:C7057 .
  
  dgn-gda:DGN0e02c1823f7396f4ef63e316ad50ce07 sio:SIO_000628 miriam-gene:4137, lld:C0949664;
    a sio:SIO_001121 .
}

dgn-np:NP940378.RAiEj_EGIe9Cyct8l5fNwH__c8Yi4L31jOSQoFhua3w4Q130_provenance {
  dgn-np:NP940378.RAiEj_EGIe9Cyct8l5fNwH__c8Yi4L31jOSQoFhua3w4Q130_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:NP940378.RAiEj_EGIe9Cyct8l5fNwH__c8Yi4L31jOSQoFhua3w4Q130_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;
    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" .
}