@prefix this: <http://rdf.disgenet.org/resource/nanopub/NP880776.RAjhCG6HHn6MaUmfFXZWkEP05IQ1NhO7rDFEFb6IGes20> .
@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:NP880776.RAjhCG6HHn6MaUmfFXZWkEP05IQ1NhO7rDFEFb6IGes20130_head {
  this: np:hasAssertion dgn-np:NP880776.RAjhCG6HHn6MaUmfFXZWkEP05IQ1NhO7rDFEFb6IGes20130_assertion;
    np:hasProvenance dgn-np:NP880776.RAjhCG6HHn6MaUmfFXZWkEP05IQ1NhO7rDFEFb6IGes20130_provenance;
    np:hasPublicationInfo dgn-np:NP880776.RAjhCG6HHn6MaUmfFXZWkEP05IQ1NhO7rDFEFb6IGes20130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP880776.RAjhCG6HHn6MaUmfFXZWkEP05IQ1NhO7rDFEFb6IGes20130_assertion a np:Assertion .
  
  dgn-np:NP880776.RAjhCG6HHn6MaUmfFXZWkEP05IQ1NhO7rDFEFb6IGes20130_provenance a np:Provenance .
  
  dgn-np:NP880776.RAjhCG6HHn6MaUmfFXZWkEP05IQ1NhO7rDFEFb6IGes20130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP880776.RAjhCG6HHn6MaUmfFXZWkEP05IQ1NhO7rDFEFb6IGes20130_assertion {
  miriam-gene:25978 a ncit:C16612 .
  
  lld:C0338451 a ncit:C7057 .
  
  dgn-gda:DGN8eccb7ced471c5c2535f6dc5f2c7d59b sio:SIO_000628 miriam-gene:25978, lld:C0338451;
    a sio:SIO_001121 .
}

dgn-np:NP880776.RAjhCG6HHn6MaUmfFXZWkEP05IQ1NhO7rDFEFb6IGes20130_provenance {
  dgn-np:NP880776.RAjhCG6HHn6MaUmfFXZWkEP05IQ1NhO7rDFEFb6IGes20130_assertion dcterms:description
      "[Mutations in 7 known genes (MAPT, GRN, C9orf72, VCP, CHMP2B, and, rarely, TARDBP and FUS) are associated with frontotemporal dementia, and the pathologic classification of frontotemporal lobar degeneration has recently been modified to reflect these discoveries.]. 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:24709683;
    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:NP880776.RAjhCG6HHn6MaUmfFXZWkEP05IQ1NhO7rDFEFb6IGes20130_publicationInfo {
  this: dcterms:created "2015-08-25T14:46:36+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" .
}