@prefix this: <http://rdf.disgenet.org/resource/nanopub/NP872789.RAMRFpEXbW491yITLO559_sEt-9SVNQzzrebI9AWz_cQc> .
@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:NP872789.RAMRFpEXbW491yITLO559_sEt-9SVNQzzrebI9AWz_cQc130_head {
  this: np:hasAssertion dgn-np:NP872789.RAMRFpEXbW491yITLO559_sEt-9SVNQzzrebI9AWz_cQc130_assertion;
    np:hasProvenance dgn-np:NP872789.RAMRFpEXbW491yITLO559_sEt-9SVNQzzrebI9AWz_cQc130_provenance;
    np:hasPublicationInfo dgn-np:NP872789.RAMRFpEXbW491yITLO559_sEt-9SVNQzzrebI9AWz_cQc130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP872789.RAMRFpEXbW491yITLO559_sEt-9SVNQzzrebI9AWz_cQc130_assertion a np:Assertion .
  
  dgn-np:NP872789.RAMRFpEXbW491yITLO559_sEt-9SVNQzzrebI9AWz_cQc130_provenance a np:Provenance .
  
  dgn-np:NP872789.RAMRFpEXbW491yITLO559_sEt-9SVNQzzrebI9AWz_cQc130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP872789.RAMRFpEXbW491yITLO559_sEt-9SVNQzzrebI9AWz_cQc130_assertion {
  miriam-gene:23435 a ncit:C16612 .
  
  lld:C0234133 a ncit:C7057 .
  
  dgn-gda:DGNda4c20af7c3d7a241cc717d4998f14cf sio:SIO_000628 miriam-gene:23435, lld:C0234133;
    a sio:SIO_001122 .
}

dgn-np:NP872789.RAMRFpEXbW491yITLO559_sEt-9SVNQzzrebI9AWz_cQc130_provenance {
  dgn-np:NP872789.RAMRFpEXbW491yITLO559_sEt-9SVNQzzrebI9AWz_cQc130_assertion dcterms:description
      "[Our findings suggest that the clinical presentation of the p.A382T TARDBP gene mutation may include forms of parkinsonism in which the extrapyramidal signs are the crucial core of the disease at onset.]. 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:23546887;
    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:NP872789.RAMRFpEXbW491yITLO559_sEt-9SVNQzzrebI9AWz_cQc130_publicationInfo {
  this: dcterms:created "2015-08-25T14:46:31+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" .
}