@prefix this: <http://rdf.disgenet.org/resource/nanopub/NP1112056.RAqn_e0IVuACEhQzn2wBpYREODdSvS0MJIJiRMoVbC8vg> .
@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:NP1112056.RAqn_e0IVuACEhQzn2wBpYREODdSvS0MJIJiRMoVbC8vg130_head {
  this: np:hasAssertion dgn-np:NP1112056.RAqn_e0IVuACEhQzn2wBpYREODdSvS0MJIJiRMoVbC8vg130_assertion;
    np:hasProvenance dgn-np:NP1112056.RAqn_e0IVuACEhQzn2wBpYREODdSvS0MJIJiRMoVbC8vg130_provenance;
    np:hasPublicationInfo dgn-np:NP1112056.RAqn_e0IVuACEhQzn2wBpYREODdSvS0MJIJiRMoVbC8vg130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP1112056.RAqn_e0IVuACEhQzn2wBpYREODdSvS0MJIJiRMoVbC8vg130_assertion a np:Assertion .
  
  dgn-np:NP1112056.RAqn_e0IVuACEhQzn2wBpYREODdSvS0MJIJiRMoVbC8vg130_provenance a np:Provenance .
  
  dgn-np:NP1112056.RAqn_e0IVuACEhQzn2wBpYREODdSvS0MJIJiRMoVbC8vg130_publicationInfo
    a np:PublicationInfo .
}

dgn-np:NP1112056.RAqn_e0IVuACEhQzn2wBpYREODdSvS0MJIJiRMoVbC8vg130_assertion {
  miriam-gene:4137 a ncit:C16612 .
  
  lld:C0949664 a ncit:C7057 .
  
  dgn-gda:DGNe3d957ab56a3c7afbcca444396eae4ba sio:SIO_000628 miriam-gene:4137, lld:C0949664;
    a sio:SIO_001121 .
}

dgn-np:NP1112056.RAqn_e0IVuACEhQzn2wBpYREODdSvS0MJIJiRMoVbC8vg130_provenance {
  dgn-np:NP1112056.RAqn_e0IVuACEhQzn2wBpYREODdSvS0MJIJiRMoVbC8vg130_assertion dcterms:description
      "[However, the existence of tauopathies that are devoid of Aβ deposits, together with the discovery of mutations in the tau gene leading to frontotemporal dementia with parkinsonism linked to chromosome 17 (FTDP-17T), confirmed the importance of tau per se in disease.]. 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:24050961;
    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:NP1112056.RAqn_e0IVuACEhQzn2wBpYREODdSvS0MJIJiRMoVbC8vg130_publicationInfo {
  this: dcterms:created "2016-05-13T12:50:10+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" .
}