@prefix this: <http://rdf.disgenet.org/resource/nanopub/NP763490.RAy_xQll16gRZYvqDTQYnzVZAtycCsDxTrYJpOIcf1a9Y> .
@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:NP763490.RAy_xQll16gRZYvqDTQYnzVZAtycCsDxTrYJpOIcf1a9Y130_head {
  this: np:hasAssertion dgn-np:NP763490.RAy_xQll16gRZYvqDTQYnzVZAtycCsDxTrYJpOIcf1a9Y130_assertion;
    np:hasProvenance dgn-np:NP763490.RAy_xQll16gRZYvqDTQYnzVZAtycCsDxTrYJpOIcf1a9Y130_provenance;
    np:hasPublicationInfo dgn-np:NP763490.RAy_xQll16gRZYvqDTQYnzVZAtycCsDxTrYJpOIcf1a9Y130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP763490.RAy_xQll16gRZYvqDTQYnzVZAtycCsDxTrYJpOIcf1a9Y130_assertion a np:Assertion .
  
  dgn-np:NP763490.RAy_xQll16gRZYvqDTQYnzVZAtycCsDxTrYJpOIcf1a9Y130_provenance a np:Provenance .
  
  dgn-np:NP763490.RAy_xQll16gRZYvqDTQYnzVZAtycCsDxTrYJpOIcf1a9Y130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP763490.RAy_xQll16gRZYvqDTQYnzVZAtycCsDxTrYJpOIcf1a9Y130_assertion {
  miriam-gene:23400 a ncit:C16612 .
  
  lld:C0242422 a ncit:C7057 .
  
  dgn-gda:DGNad1b2104ab5aa104fd0b8981a50222c8 sio:SIO_000628 miriam-gene:23400, lld:C0242422;
    a sio:SIO_001121 .
}

dgn-np:NP763490.RAy_xQll16gRZYvqDTQYnzVZAtycCsDxTrYJpOIcf1a9Y130_provenance {
  dgn-np:NP763490.RAy_xQll16gRZYvqDTQYnzVZAtycCsDxTrYJpOIcf1a9Y130_assertion dcterms:description
      "[As noted in this review, there appears to be common threads between the two disorders, as mutations in the genes, parkin and ATP13A2, associated with early onset of Parkinsonism, may also predispose an individual to develop Mn toxicity.]. 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:19757210;
    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:NP763490.RAy_xQll16gRZYvqDTQYnzVZAtycCsDxTrYJpOIcf1a9Y130_publicationInfo {
  this: dcterms:created "2016-05-13T12:47:31+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 "v4.0.0.0" .
  
  dgn-void:disgenetv3.0rdf pav:version "v4.0.0" .
}