@prefix this: <http://rdf.disgenet.org/resource/nanopub/NP814750.RAltC_ZA8fp5sc8Luy1TP_DBs5jiUMkQQkLzx7hj9ySDE> .
@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:NP814750.RAltC_ZA8fp5sc8Luy1TP_DBs5jiUMkQQkLzx7hj9ySDE130_head {
  this: np:hasAssertion dgn-np:NP814750.RAltC_ZA8fp5sc8Luy1TP_DBs5jiUMkQQkLzx7hj9ySDE130_assertion;
    np:hasProvenance dgn-np:NP814750.RAltC_ZA8fp5sc8Luy1TP_DBs5jiUMkQQkLzx7hj9ySDE130_provenance;
    np:hasPublicationInfo dgn-np:NP814750.RAltC_ZA8fp5sc8Luy1TP_DBs5jiUMkQQkLzx7hj9ySDE130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP814750.RAltC_ZA8fp5sc8Luy1TP_DBs5jiUMkQQkLzx7hj9ySDE130_assertion a np:Assertion .
  
  dgn-np:NP814750.RAltC_ZA8fp5sc8Luy1TP_DBs5jiUMkQQkLzx7hj9ySDE130_provenance a np:Provenance .
  
  dgn-np:NP814750.RAltC_ZA8fp5sc8Luy1TP_DBs5jiUMkQQkLzx7hj9ySDE130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP814750.RAltC_ZA8fp5sc8Luy1TP_DBs5jiUMkQQkLzx7hj9ySDE130_assertion {
  miriam-gene:4287 a ncit:C16612 .
  
  lld:C0024408 a ncit:C7057 .
  
  dgn-gda:DGN64c52cae82f3fdc060ef28506133a461 sio:SIO_000628 miriam-gene:4287, lld:C0024408;
    a sio:SIO_001121 .
}

dgn-np:NP814750.RAltC_ZA8fp5sc8Luy1TP_DBs5jiUMkQQkLzx7hj9ySDE130_provenance {
  dgn-np:NP814750.RAltC_ZA8fp5sc8Luy1TP_DBs5jiUMkQQkLzx7hj9ySDE130_assertion dcterms:description
      "[Machado-Joseph disease (MJD) is an autosomal dominant neurodegenerative disease caused by an expansion of CAG repeats in the MJD1 gene, in which lower urinary tract dysfunction is known to be the most commonly encountered autonomic failure.]. 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:20503052;
    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:NP814750.RAltC_ZA8fp5sc8Luy1TP_DBs5jiUMkQQkLzx7hj9ySDE130_publicationInfo {
  this: dcterms:created "2016-05-13T12:47:54+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" .
}