@prefix this: <http://rdf.disgenet.org/resource/nanopub/NP10249.RAsugkvd1XJmx5crZWSy8gPkVHAwrdZbAkoujBE00l6kw> .
@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:NP10249.RAsugkvd1XJmx5crZWSy8gPkVHAwrdZbAkoujBE00l6kw130_head {
  this: np:hasAssertion dgn-np:NP10249.RAsugkvd1XJmx5crZWSy8gPkVHAwrdZbAkoujBE00l6kw130_assertion;
    np:hasProvenance dgn-np:NP10249.RAsugkvd1XJmx5crZWSy8gPkVHAwrdZbAkoujBE00l6kw130_provenance;
    np:hasPublicationInfo dgn-np:NP10249.RAsugkvd1XJmx5crZWSy8gPkVHAwrdZbAkoujBE00l6kw130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP10249.RAsugkvd1XJmx5crZWSy8gPkVHAwrdZbAkoujBE00l6kw130_assertion a np:Assertion .
  
  dgn-np:NP10249.RAsugkvd1XJmx5crZWSy8gPkVHAwrdZbAkoujBE00l6kw130_provenance a np:Provenance .
  
  dgn-np:NP10249.RAsugkvd1XJmx5crZWSy8gPkVHAwrdZbAkoujBE00l6kw130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP10249.RAsugkvd1XJmx5crZWSy8gPkVHAwrdZbAkoujBE00l6kw130_assertion {
  miriam-gene:5071 a ncit:C16612 .
  
  lld:C0242422 a ncit:C7057 .
  
  dgn-gda:DGNa8420a6ec41a0e97a1560b7793813cb8 sio:SIO_000628 miriam-gene:5071, lld:C0242422;
    a sio:SIO_001121 .
}

dgn-np:NP10249.RAsugkvd1XJmx5crZWSy8gPkVHAwrdZbAkoujBE00l6kw130_provenance {
  dgn-np:NP10249.RAsugkvd1XJmx5crZWSy8gPkVHAwrdZbAkoujBE00l6kw130_assertion dcterms:description
      "[A wide variety of mutations in the parkin gene are responsible for autosomal recessive parkinsonism in Europe. French Parkinson's Disease Genetics Study Group and the European Consortium on Genetic Susceptibility in Parkinson's Disease.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en;
    wi:evidence dgn-void:source_evidence_curated;
    sio:SIO_000772 miriam-pubmed:10072423;
    prov:wasDerivedFrom dgn-void:ctd_human-2016;
    prov:wasGeneratedBy eco:ECO_0000218 .
  
  dgn-void:ctd_human-2016 pav:importedOn "2016-01-25"^^xsd:date .
  
  dgn-void:source_evidence_curated a eco:ECO_0000205;
    rdfs:comment "Gene-disease associations manually curated."@en;
    rdfs:label "DisGeNET evidence - CURATED"@en .
}

dgn-np:NP10249.RAsugkvd1XJmx5crZWSy8gPkVHAwrdZbAkoujBE00l6kw130_publicationInfo {
  this: dcterms:created "2016-05-13T12:41:54+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" .
}