@prefix this: <http://rdf.disgenet.org/resource/nanopub/NP308559.RADBhFlIMU_vm15XGZqDLuApzzs9nzGKehCHR2yFzCvTc> .
@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:NP308559.RADBhFlIMU_vm15XGZqDLuApzzs9nzGKehCHR2yFzCvTc130_head {
  this: np:hasAssertion dgn-np:NP308559.RADBhFlIMU_vm15XGZqDLuApzzs9nzGKehCHR2yFzCvTc130_assertion;
    np:hasProvenance dgn-np:NP308559.RADBhFlIMU_vm15XGZqDLuApzzs9nzGKehCHR2yFzCvTc130_provenance;
    np:hasPublicationInfo dgn-np:NP308559.RADBhFlIMU_vm15XGZqDLuApzzs9nzGKehCHR2yFzCvTc130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP308559.RADBhFlIMU_vm15XGZqDLuApzzs9nzGKehCHR2yFzCvTc130_assertion a np:Assertion .
  
  dgn-np:NP308559.RADBhFlIMU_vm15XGZqDLuApzzs9nzGKehCHR2yFzCvTc130_provenance a np:Provenance .
  
  dgn-np:NP308559.RADBhFlIMU_vm15XGZqDLuApzzs9nzGKehCHR2yFzCvTc130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP308559.RADBhFlIMU_vm15XGZqDLuApzzs9nzGKehCHR2yFzCvTc130_assertion {
  miriam-gene:4137 a ncit:C16612 .
  
  lld:C0338451 a ncit:C7057 .
  
  dgn-gda:DGN6b6d5ae382ef83b0a108792af1b25f62 sio:SIO_000628 miriam-gene:4137, lld:C0338451;
    a sio:SIO_001121 .
}

dgn-np:NP308559.RADBhFlIMU_vm15XGZqDLuApzzs9nzGKehCHR2yFzCvTc130_provenance {
  dgn-np:NP308559.RADBhFlIMU_vm15XGZqDLuApzzs9nzGKehCHR2yFzCvTc130_assertion dcterms:description
      "[The discovery of multiple tau gene mutations that are pathogenic for hereditary frontotemporal dementia and parkinsonism linked to chromosome 17 in many kindreds, as well as the demonstration that tau polymorphisms are genetic risk factors for sporadic tauopathies, directly implicate tau abnormalities in the onset/progression of neurodegenerative disease.]. 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:11207421;
    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:NP308559.RADBhFlIMU_vm15XGZqDLuApzzs9nzGKehCHR2yFzCvTc130_publicationInfo {
  this: dcterms:created "2016-05-13T12:44:05+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" .
}