@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP906230.RA48pmvP67dWapQh4msnrcuKbmSULW42Fn80YooFurNoo> .
@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/eco.owl#> .
@prefix wi: <http://purl.org/ontology/wi/core#> .
@prefix prov: <http://www.w3.org/ns/prov#> .
@prefix pav: <http://purl.org/pav/2.0/> .
@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/nanopublications.trig#> .
@prefix dgn-gda: <http://rdf.disgenet.org/gene-disease-association.ttl#> .
@prefix dgn-void: <http://rdf.disgenet.org/v2.1.0/void.ttl#> .

dgn-np:NP906230.RA48pmvP67dWapQh4msnrcuKbmSULW42Fn80YooFurNoo130_head {
  this: np:hasAssertion dgn-np:NP906230.RA48pmvP67dWapQh4msnrcuKbmSULW42Fn80YooFurNoo130_assertion;
    np:hasProvenance dgn-np:NP906230.RA48pmvP67dWapQh4msnrcuKbmSULW42Fn80YooFurNoo130_provenance;
    np:hasPublicationInfo dgn-np:NP906230.RA48pmvP67dWapQh4msnrcuKbmSULW42Fn80YooFurNoo130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP906230.RA48pmvP67dWapQh4msnrcuKbmSULW42Fn80YooFurNoo130_assertion a np:Assertion .
  
  dgn-np:NP906230.RA48pmvP67dWapQh4msnrcuKbmSULW42Fn80YooFurNoo130_provenance a np:Provenance .
  
  dgn-np:NP906230.RA48pmvP67dWapQh4msnrcuKbmSULW42Fn80YooFurNoo130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP906230.RA48pmvP67dWapQh4msnrcuKbmSULW42Fn80YooFurNoo130_assertion {
  miriam-gene:4137 a ncit:C16612 .
  
  lld:C0037019 a ncit:C7057 .
  
  dgn-gda:DGN79c99a01f073a05e70201092b5941d6e sio:SIO_000628 miriam-gene:4137, lld:C0037019;
    a sio:SIO_001121 .
}

dgn-np:NP906230.RA48pmvP67dWapQh4msnrcuKbmSULW42Fn80YooFurNoo130_provenance {
  dgn-np:NP906230.RA48pmvP67dWapQh4msnrcuKbmSULW42Fn80YooFurNoo130_assertion dcterms:description
      "[Mutations in the microtubule-associated protein tau gene (MAPT) can cause frontotemporal dementia with Parkinsonism linked to the chromosome 17, and are associated with the risk for progressive supranuclear palsy, Parkinson's disease, corticobasal degeneration, and multiple system atrophy.]. 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:23001634;
    prov:wasDerivedFrom dgn-void:befree-20140225;
    prov:wasGeneratedBy eco:ECO_0000203 .
  
  dgn-void:befree-20140225 pav:importedOn "2014-02-25"^^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:NP906230.RA48pmvP67dWapQh4msnrcuKbmSULW42Fn80YooFurNoo130_publicationInfo {
  this: dcterms:created "2014-10-02T12:41:16+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:disgenetrdf;
    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 "v2.1.0.0" .
  
  dgn-void:disgenetrdf pav:version "v2.1.0" .
}