@prefix this: <http://rdf.disgenet.org/resource/nanopub/NP706178.RAl8IoMejreKg6q1Qt9Y89i0f4BgXc8gxh7VkFItsngLI> .
@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:NP706178.RAl8IoMejreKg6q1Qt9Y89i0f4BgXc8gxh7VkFItsngLI130_head {
  this: np:hasAssertion dgn-np:NP706178.RAl8IoMejreKg6q1Qt9Y89i0f4BgXc8gxh7VkFItsngLI130_assertion;
    np:hasProvenance dgn-np:NP706178.RAl8IoMejreKg6q1Qt9Y89i0f4BgXc8gxh7VkFItsngLI130_provenance;
    np:hasPublicationInfo dgn-np:NP706178.RAl8IoMejreKg6q1Qt9Y89i0f4BgXc8gxh7VkFItsngLI130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP706178.RAl8IoMejreKg6q1Qt9Y89i0f4BgXc8gxh7VkFItsngLI130_assertion a np:Assertion .
  
  dgn-np:NP706178.RAl8IoMejreKg6q1Qt9Y89i0f4BgXc8gxh7VkFItsngLI130_provenance a np:Provenance .
  
  dgn-np:NP706178.RAl8IoMejreKg6q1Qt9Y89i0f4BgXc8gxh7VkFItsngLI130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP706178.RAl8IoMejreKg6q1Qt9Y89i0f4BgXc8gxh7VkFItsngLI130_assertion {
  miriam-gene:1861 a ncit:C16612 .
  
  lld:C0393593 a ncit:C7057 .
  
  dgn-gda:DGN8342d5fb45ae63281b3cad8d68458d83 sio:SIO_000628 miriam-gene:1861, lld:C0393593;
    a sio:SIO_001121 .
}

dgn-np:NP706178.RAl8IoMejreKg6q1Qt9Y89i0f4BgXc8gxh7VkFItsngLI130_provenance {
  dgn-np:NP706178.RAl8IoMejreKg6q1Qt9Y89i0f4BgXc8gxh7VkFItsngLI130_assertion dcterms:description
      "[Moreover, dystonia and Parkinson disease share the common feature of reduced dopamine neurotransmission in the striatum, so we assumed that mutations in the DYT1 gene might have the same role in cases of early onset primary torsion dystonia (EOPTD) and early onset Parkinson disease (EOPD) that present dystonia.]. 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:19038309;
    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:NP706178.RAl8IoMejreKg6q1Qt9Y89i0f4BgXc8gxh7VkFItsngLI130_publicationInfo {
  this: dcterms:created "2016-05-13T12:47:05+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" .
}