@prefix this: <http://rdf.disgenet.org/resource/nanopub/NP546155.RAGRkiPk_YO0RE-NX06x0NutNZ2OTYleUHw-2VgwPhRUQ> .
@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/v3.0.0/void/> .
dgn-np:NP546155.RAGRkiPk_YO0RE-NX06x0NutNZ2OTYleUHw-2VgwPhRUQ130_head {
  this: np:hasAssertion dgn-np:NP546155.RAGRkiPk_YO0RE-NX06x0NutNZ2OTYleUHw-2VgwPhRUQ130_assertion ;
    np:hasProvenance dgn-np:NP546155.RAGRkiPk_YO0RE-NX06x0NutNZ2OTYleUHw-2VgwPhRUQ130_provenance ;
    np:hasPublicationInfo dgn-np:NP546155.RAGRkiPk_YO0RE-NX06x0NutNZ2OTYleUHw-2VgwPhRUQ130_publicationInfo ;
    a np:Nanopublication .
  dgn-np:NP546155.RAGRkiPk_YO0RE-NX06x0NutNZ2OTYleUHw-2VgwPhRUQ130_assertion a np:Assertion .
  dgn-np:NP546155.RAGRkiPk_YO0RE-NX06x0NutNZ2OTYleUHw-2VgwPhRUQ130_provenance a np:Provenance .
  dgn-np:NP546155.RAGRkiPk_YO0RE-NX06x0NutNZ2OTYleUHw-2VgwPhRUQ130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP546155.RAGRkiPk_YO0RE-NX06x0NutNZ2OTYleUHw-2VgwPhRUQ130_assertion {
  miriam-gene:4137 a ncit:C16612 .
  lld:C0338451 a ncit:C7057 .
  dgn-gda:DGNe4f3e74f48dfdcd43aaeeb8b576b7604 sio:SIO_000628 miriam-gene:4137 , lld:C0338451 ;
    a sio:SIO_001121 .
}
dgn-np:NP546155.RAGRkiPk_YO0RE-NX06x0NutNZ2OTYleUHw-2VgwPhRUQ130_provenance {
  dgn-np:NP546155.RAGRkiPk_YO0RE-NX06x0NutNZ2OTYleUHw-2VgwPhRUQ130_assertion dcterms:description "[Several silent and intronic mutations of the tau gene associated with FTDP-17T (frontotemporal dementia with Parkinsonism linked to chromosome 17 and specifically characterized by tau pathology) only disrupt exon 10 splicing, but do not influence the primary sequence of the tau protein.]. 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:24627328 ;
    prov:wasDerivedFrom dgn-void:befree-20150227 ;
    prov:wasGeneratedBy eco:ECO_0000203 .
  dgn-void:befree-20150227 pav:importedOn "2015-02-27"^^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:NP546155.RAGRkiPk_YO0RE-NX06x0NutNZ2OTYleUHw-2VgwPhRUQ130_publicationInfo {
  this: dcterms:created "2015-08-25T14:43:03+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 "v3.0.0.0" .
  dgn-void:disgenetv3.0rdf pav:version "v3.0.0" .
}