@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP61232.RA4AYELqn-lDlqH7N9pImV00xCZ-nEC6t4r4elqplCClA> .
@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:NP61232.RA4AYELqn-lDlqH7N9pImV00xCZ-nEC6t4r4elqplCClA130_head {
  this: np:hasAssertion dgn-np:NP61232.RA4AYELqn-lDlqH7N9pImV00xCZ-nEC6t4r4elqplCClA130_assertion;
    np:hasProvenance dgn-np:NP61232.RA4AYELqn-lDlqH7N9pImV00xCZ-nEC6t4r4elqplCClA130_provenance;
    np:hasPublicationInfo dgn-np:NP61232.RA4AYELqn-lDlqH7N9pImV00xCZ-nEC6t4r4elqplCClA130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP61232.RA4AYELqn-lDlqH7N9pImV00xCZ-nEC6t4r4elqplCClA130_assertion a np:Assertion .
  
  dgn-np:NP61232.RA4AYELqn-lDlqH7N9pImV00xCZ-nEC6t4r4elqplCClA130_provenance a np:Provenance .
  
  dgn-np:NP61232.RA4AYELqn-lDlqH7N9pImV00xCZ-nEC6t4r4elqplCClA130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP61232.RA4AYELqn-lDlqH7N9pImV00xCZ-nEC6t4r4elqplCClA130_assertion {
  miriam-gene:4137 a ncit:C16612 .
  
  lld:C0338451 a ncit:C7057 .
  
  dgn-gda:DGNe4d4845ba225e089f90dcaad68c1a0ef sio:SIO_000628 miriam-gene:4137, lld:C0338451;
    a sio:SIO_001122 .
}

dgn-np:NP61232.RA4AYELqn-lDlqH7N9pImV00xCZ-nEC6t4r4elqplCClA130_provenance {
  dgn-np:NP61232.RA4AYELqn-lDlqH7N9pImV00xCZ-nEC6t4r4elqplCClA130_assertion dcterms:description
      "[We conclude that  the prevalence of FTD in The Netherlands is higher than previously reported, confirming that FTD is more common than was previously thought. The finding of tau mutations in 32% of patients with a positive family history for dementia justifies mutation screening in FTD patients with a positive family history, while tau mutations in non-familiar cases are rare.]. 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:12876142;
    prov:wasDerivedFrom dgn-void:gad-20130706;
    prov:wasGeneratedBy eco:ECO_0000203 .
  
  dgn-void:gad-20130706 pav:importedOn "2013-07-06"^^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:NP61232.RA4AYELqn-lDlqH7N9pImV00xCZ-nEC6t4r4elqplCClA130_publicationInfo {
  this: dcterms:created "2014-10-02T12:32:29+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" .
}