@prefix this: <http://rdf.disgenet.org/resource/nanopub/NP557428.RAiC26qSYq3vmmywImqqALlZqm-z38rZnukQgKdNx-gNI> .
@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:NP557428.RAiC26qSYq3vmmywImqqALlZqm-z38rZnukQgKdNx-gNI130_head {
  this: np:hasAssertion dgn-np:NP557428.RAiC26qSYq3vmmywImqqALlZqm-z38rZnukQgKdNx-gNI130_assertion;
    np:hasProvenance dgn-np:NP557428.RAiC26qSYq3vmmywImqqALlZqm-z38rZnukQgKdNx-gNI130_provenance;
    np:hasPublicationInfo dgn-np:NP557428.RAiC26qSYq3vmmywImqqALlZqm-z38rZnukQgKdNx-gNI130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP557428.RAiC26qSYq3vmmywImqqALlZqm-z38rZnukQgKdNx-gNI130_assertion a np:Assertion .
  
  dgn-np:NP557428.RAiC26qSYq3vmmywImqqALlZqm-z38rZnukQgKdNx-gNI130_provenance a np:Provenance .
  
  dgn-np:NP557428.RAiC26qSYq3vmmywImqqALlZqm-z38rZnukQgKdNx-gNI130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP557428.RAiC26qSYq3vmmywImqqALlZqm-z38rZnukQgKdNx-gNI130_assertion {
  miriam-gene:4287 a ncit:C16612 .
  
  lld:C0393911 a ncit:C7057 .
  
  dgn-gda:DGN41d2e0d7bf0360c6201535e2fba80c67 sio:SIO_000628 miriam-gene:4287, lld:C0393911;
    a sio:SIO_001121 .
}

dgn-np:NP557428.RAiC26qSYq3vmmywImqqALlZqm-z38rZnukQgKdNx-gNI130_provenance {
  dgn-np:NP557428.RAiC26qSYq3vmmywImqqALlZqm-z38rZnukQgKdNx-gNI130_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-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:NP557428.RAiC26qSYq3vmmywImqqALlZqm-z38rZnukQgKdNx-gNI130_publicationInfo {
  this: dcterms:created "2015-08-25T14:43:10+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 "v3.0.0.0" .
  
  dgn-void:disgenetv3.0rdf pav:version "v3.0.0" .
}