@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP93371.RAD6jgaEW2ydqc8BsT8xvFS5ugZk3KBTidE1uMK_nlg6g> .
@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/eco.owl#> .
@prefix wi: <http://purl.org/ontology/wi/core#> .
@prefix prov: <http://www.w3.org/ns/prov#> .
@prefix pav: <http://purl.org/pav/2.0/> .
@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/nanopublications.trig#> .
@prefix dgn-gda: <http://rdf.disgenet.org/gene-disease-association.ttl#> .
@prefix dgn-void: <http://rdf.disgenet.org/v2.1.0/void.ttl#> .

dgn-np:NP93371.RAD6jgaEW2ydqc8BsT8xvFS5ugZk3KBTidE1uMK_nlg6g130_head {
  this: np:hasAssertion dgn-np:NP93371.RAD6jgaEW2ydqc8BsT8xvFS5ugZk3KBTidE1uMK_nlg6g130_assertion;
    np:hasProvenance dgn-np:NP93371.RAD6jgaEW2ydqc8BsT8xvFS5ugZk3KBTidE1uMK_nlg6g130_provenance;
    np:hasPublicationInfo dgn-np:NP93371.RAD6jgaEW2ydqc8BsT8xvFS5ugZk3KBTidE1uMK_nlg6g130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP93371.RAD6jgaEW2ydqc8BsT8xvFS5ugZk3KBTidE1uMK_nlg6g130_assertion a np:Assertion .
  
  dgn-np:NP93371.RAD6jgaEW2ydqc8BsT8xvFS5ugZk3KBTidE1uMK_nlg6g130_provenance a np:Provenance .
  
  dgn-np:NP93371.RAD6jgaEW2ydqc8BsT8xvFS5ugZk3KBTidE1uMK_nlg6g130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP93371.RAD6jgaEW2ydqc8BsT8xvFS5ugZk3KBTidE1uMK_nlg6g130_assertion {
  miriam-gene:165829 a ncit:C16612 .
  
  lld:C0030567 a ncit:C7057 .
  
  dgn-gda:DGNed35e21d420ec857a00a26c09bdda5c9 sio:SIO_000628 miriam-gene:165829, lld:C0030567;
    a sio:SIO_001122 .
}

dgn-np:NP93371.RAD6jgaEW2ydqc8BsT8xvFS5ugZk3KBTidE1uMK_nlg6g130_provenance {
  dgn-np:NP93371.RAD6jgaEW2ydqc8BsT8xvFS5ugZk3KBTidE1uMK_nlg6g130_assertion dcterms:description
      "[We generated publicly available genotype data for Parkinsons disease patients and controls so that these data can be mined and augmented by other researchers to identify common genetic variability that results in minor and moderate risk for disease.]. 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:17052657;
    prov:wasDerivedFrom dgn-void:gad-20130706;
    prov:wasGeneratedBy eco:ECO_0000203 .
  
  dgn-void:gad-20130706 pav:importedOn "2013-07-06"^^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:NP93371.RAD6jgaEW2ydqc8BsT8xvFS5ugZk3KBTidE1uMK_nlg6g130_publicationInfo {
  this: dcterms:created "2014-10-02T12:32:46+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:disgenetrdf;
    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 "v2.1.0.0" .
  
  dgn-void:disgenetrdf pav:version "v2.1.0" .
}