@prefix this: <http://rdf.disgenet.org/resource/nanopub/NP406638.RAAO2rXRBurNXxI76Vpp3v7qVVu92BufmCK9nnYBV-m-0> .
@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:NP406638.RAAO2rXRBurNXxI76Vpp3v7qVVu92BufmCK9nnYBV-m-0130_head {
  this: np:hasAssertion dgn-np:NP406638.RAAO2rXRBurNXxI76Vpp3v7qVVu92BufmCK9nnYBV-m-0130_assertion;
    np:hasProvenance dgn-np:NP406638.RAAO2rXRBurNXxI76Vpp3v7qVVu92BufmCK9nnYBV-m-0130_provenance;
    np:hasPublicationInfo dgn-np:NP406638.RAAO2rXRBurNXxI76Vpp3v7qVVu92BufmCK9nnYBV-m-0130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP406638.RAAO2rXRBurNXxI76Vpp3v7qVVu92BufmCK9nnYBV-m-0130_assertion a np:Assertion .
  
  dgn-np:NP406638.RAAO2rXRBurNXxI76Vpp3v7qVVu92BufmCK9nnYBV-m-0130_provenance a np:Provenance .
  
  dgn-np:NP406638.RAAO2rXRBurNXxI76Vpp3v7qVVu92BufmCK9nnYBV-m-0130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP406638.RAAO2rXRBurNXxI76Vpp3v7qVVu92BufmCK9nnYBV-m-0130_assertion {
  miriam-gene:4137 a ncit:C16612 .
  
  lld:C0338451 a ncit:C7057 .
  
  dgn-gda:DGN1c4b1a0be94702ae64b209ef1c4e695d sio:SIO_000628 miriam-gene:4137, lld:C0338451;
    a sio:SIO_001121 .
}

dgn-np:NP406638.RAAO2rXRBurNXxI76Vpp3v7qVVu92BufmCK9nnYBV-m-0130_provenance {
  dgn-np:NP406638.RAAO2rXRBurNXxI76Vpp3v7qVVu92BufmCK9nnYBV-m-0130_assertion dcterms:description
      "[The second part will deal with the recent discovery of tau gene mutations in frontotemporal dementia and parkinsonism linked to chromosome 17 which demonstrates that tau dysfunction can lead to neurodegeneration.]. 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:12938731;
    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:NP406638.RAAO2rXRBurNXxI76Vpp3v7qVVu92BufmCK9nnYBV-m-0130_publicationInfo {
  this: dcterms:created "2016-05-13T12:44:49+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" .
}