@prefix this: <http://rdf.disgenet.org/resource/nanopub/NP1276518.RAkWAGT494Yb_YyAXR6FnonryczLesMHO039TnxnqlzTo> .
@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:NP1276518.RAkWAGT494Yb_YyAXR6FnonryczLesMHO039TnxnqlzTo130_head {
  this: np:hasAssertion dgn-np:NP1276518.RAkWAGT494Yb_YyAXR6FnonryczLesMHO039TnxnqlzTo130_assertion;
    np:hasProvenance dgn-np:NP1276518.RAkWAGT494Yb_YyAXR6FnonryczLesMHO039TnxnqlzTo130_provenance;
    np:hasPublicationInfo dgn-np:NP1276518.RAkWAGT494Yb_YyAXR6FnonryczLesMHO039TnxnqlzTo130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP1276518.RAkWAGT494Yb_YyAXR6FnonryczLesMHO039TnxnqlzTo130_assertion a np:Assertion .
  
  dgn-np:NP1276518.RAkWAGT494Yb_YyAXR6FnonryczLesMHO039TnxnqlzTo130_provenance a np:Provenance .
  
  dgn-np:NP1276518.RAkWAGT494Yb_YyAXR6FnonryczLesMHO039TnxnqlzTo130_publicationInfo
    a np:PublicationInfo .
}

dgn-np:NP1276518.RAkWAGT494Yb_YyAXR6FnonryczLesMHO039TnxnqlzTo130_assertion {
  miriam-gene:23435 a ncit:C16612 .
  
  lld:C0338451 a ncit:C7057 .
  
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    a sio:SIO_001121 .
}

dgn-np:NP1276518.RAkWAGT494Yb_YyAXR6FnonryczLesMHO039TnxnqlzTo130_provenance {
  dgn-np:NP1276518.RAkWAGT494Yb_YyAXR6FnonryczLesMHO039TnxnqlzTo130_assertion dcterms:description
      "[TARDBP mutation screening should be considered in familial frontotemporal dementia cases, even without signs or symptoms of motor neuron disease, especially when other more frequent causes of genetic frontotemporal dementia (i.e.]. 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:25853458;
    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:NP1276518.RAkWAGT494Yb_YyAXR6FnonryczLesMHO039TnxnqlzTo130_publicationInfo {
  this: dcterms:created "2016-05-13T12:51:24+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" .
}