@prefix this: <http://rdf.disgenet.org/resource/nanopub/NP690037.RAWL8TFUQJ767JGUJMlVTmqCDuUFaN7eWzqneteQF-3B8> .
@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:NP690037.RAWL8TFUQJ767JGUJMlVTmqCDuUFaN7eWzqneteQF-3B8130_head {
  this: np:hasAssertion dgn-np:NP690037.RAWL8TFUQJ767JGUJMlVTmqCDuUFaN7eWzqneteQF-3B8130_assertion;
    np:hasProvenance dgn-np:NP690037.RAWL8TFUQJ767JGUJMlVTmqCDuUFaN7eWzqneteQF-3B8130_provenance;
    np:hasPublicationInfo dgn-np:NP690037.RAWL8TFUQJ767JGUJMlVTmqCDuUFaN7eWzqneteQF-3B8130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP690037.RAWL8TFUQJ767JGUJMlVTmqCDuUFaN7eWzqneteQF-3B8130_assertion a np:Assertion .
  
  dgn-np:NP690037.RAWL8TFUQJ767JGUJMlVTmqCDuUFaN7eWzqneteQF-3B8130_provenance a np:Provenance .
  
  dgn-np:NP690037.RAWL8TFUQJ767JGUJMlVTmqCDuUFaN7eWzqneteQF-3B8130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP690037.RAWL8TFUQJ767JGUJMlVTmqCDuUFaN7eWzqneteQF-3B8130_assertion {
  miriam-gene:2643 a ncit:C16612 .
  
  lld:C0393593 a ncit:C7057 .
  
  dgn-gda:DGN9932ba09ec8283ef28d79e7d90dfc1da sio:SIO_000628 miriam-gene:2643, lld:C0393593;
    a sio:SIO_001121 .
}

dgn-np:NP690037.RAWL8TFUQJ767JGUJMlVTmqCDuUFaN7eWzqneteQF-3B8130_provenance {
  dgn-np:NP690037.RAWL8TFUQJ767JGUJMlVTmqCDuUFaN7eWzqneteQF-3B8130_assertion dcterms:description
      "[Dopa-responsive dystonia (DRD), also known as Segawa syndrome or hereditary progressive dystonia with diurnal fluctuation, is clinically characterized by the occurrence of simultaneous or late Parkinsonism and by an excellent response to treatment with low doses of L-dopa.]. 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:18752196;
    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:NP690037.RAWL8TFUQJ767JGUJMlVTmqCDuUFaN7eWzqneteQF-3B8130_publicationInfo {
  this: dcterms:created "2016-05-13T12:46:58+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" .
}