@prefix dcterms: <http://purl.org/dc/terms/> .
@prefix orcid: <http://orcid.org/> .
@prefix this: <http://rdf.disgenet.org/resource/nanopub/NP36.RArBbFbaETF1r94SEwkLNHJG7kNudLtSZgNSuCFetbJaY> .
@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 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:NP36.RArBbFbaETF1r94SEwkLNHJG7kNudLtSZgNSuCFetbJaY130_head {
  this: np:hasAssertion dgn-np:NP36.RArBbFbaETF1r94SEwkLNHJG7kNudLtSZgNSuCFetbJaY130_assertion ;
    np:hasProvenance dgn-np:NP36.RArBbFbaETF1r94SEwkLNHJG7kNudLtSZgNSuCFetbJaY130_provenance ;
    np:hasPublicationInfo dgn-np:NP36.RArBbFbaETF1r94SEwkLNHJG7kNudLtSZgNSuCFetbJaY130_publicationInfo ;
    a np:Nanopublication .
  dgn-np:NP36.RArBbFbaETF1r94SEwkLNHJG7kNudLtSZgNSuCFetbJaY130_assertion a np:Assertion .
  dgn-np:NP36.RArBbFbaETF1r94SEwkLNHJG7kNudLtSZgNSuCFetbJaY130_provenance a np:Provenance .
  dgn-np:NP36.RArBbFbaETF1r94SEwkLNHJG7kNudLtSZgNSuCFetbJaY130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP36.RArBbFbaETF1r94SEwkLNHJG7kNudLtSZgNSuCFetbJaY130_assertion {
  miriam-gene:5071 a ncit:C16612 .
  lld:C3160718 a ncit:C7057 .
  dgn-gda:DGN67182c755ac8dc348f20e6ed279487bf sio:SIO_000628 miriam-gene:5071 , lld:C3160718 ;
    a sio:SIO_001122 .
}
dgn-np:NP36.RArBbFbaETF1r94SEwkLNHJG7kNudLtSZgNSuCFetbJaY130_provenance {
  dgn-np:NP36.RArBbFbaETF1r94SEwkLNHJG7kNudLtSZgNSuCFetbJaY130_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:uniprot-2016 ;
    prov:wasGeneratedBy eco:ECO_0000218 .
  dgn-void:source_evidence_curated a eco:ECO_0000205 ;
    rdfs:comment "Gene-disease associations manually curated."@en ;
    rdfs:label "DisGeNET evidence - CURATED"@en .
  dgn-void:uniprot-2016 pav:importedOn "2016-01-25"^^xsd:date .
}
dgn-np:NP36.RArBbFbaETF1r94SEwkLNHJG7kNudLtSZgNSuCFetbJaY130_publicationInfo {
  this: dcterms:created "2016-05-13T12:41:50+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 orcid:0000-0001-5999-6269 , orcid:0000-0002-7534-7661 , orcid:0000-0002-9383-528X , orcid:0000-0003-0169-8159 , orcid:0000-0003-1244-7654 ;
    pav:createdBy orcid:0000-0003-0169-8159 ;
    pav:version "v4.0.0.0" .
  dgn-void:disgenetv3.0rdf pav:version "v4.0.0" .
}