@prefix dct: <http://purl.org/dc/terms/> .
@prefix orcid: <http://orcid.org/> .
@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP78647.RA3IW9xu0pGyNTGwdFmuVoIlgFz4XITTrPXLIE2OHjSH4> .
@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 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:NP78647.RA3IW9xu0pGyNTGwdFmuVoIlgFz4XITTrPXLIE2OHjSH4130_head {
  this: np:hasAssertion dgn-np:NP78647.RA3IW9xu0pGyNTGwdFmuVoIlgFz4XITTrPXLIE2OHjSH4130_assertion;
    np:hasProvenance dgn-np:NP78647.RA3IW9xu0pGyNTGwdFmuVoIlgFz4XITTrPXLIE2OHjSH4130_provenance;
    np:hasPublicationInfo dgn-np:NP78647.RA3IW9xu0pGyNTGwdFmuVoIlgFz4XITTrPXLIE2OHjSH4130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP78647.RA3IW9xu0pGyNTGwdFmuVoIlgFz4XITTrPXLIE2OHjSH4130_assertion a np:Assertion .
  
  dgn-np:NP78647.RA3IW9xu0pGyNTGwdFmuVoIlgFz4XITTrPXLIE2OHjSH4130_provenance a np:Provenance .
  
  dgn-np:NP78647.RA3IW9xu0pGyNTGwdFmuVoIlgFz4XITTrPXLIE2OHjSH4130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP78647.RA3IW9xu0pGyNTGwdFmuVoIlgFz4XITTrPXLIE2OHjSH4130_assertion {
  miriam-gene:23127 a ncit:C16612 .
  
  lld:C0030567 a ncit:C7057 .
  
  dgn-gda:DGN396b9ed06390379216b01ce8a9b25ee8 sio:SIO_000628 miriam-gene:23127, lld:C0030567;
    a sio:SIO_001122 .
}

dgn-np:NP78647.RA3IW9xu0pGyNTGwdFmuVoIlgFz4XITTrPXLIE2OHjSH4130_provenance {
  dgn-np:NP78647.RA3IW9xu0pGyNTGwdFmuVoIlgFz4XITTrPXLIE2OHjSH4130_assertion dct: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:NP78647.RA3IW9xu0pGyNTGwdFmuVoIlgFz4XITTrPXLIE2OHjSH4130_publicationInfo {
  this: dct:created "2014-10-02T12:32:38+02:00"^^xsd:dateTime;
    dct:rights <http://opendatacommons.org/licenses/odbl/1.0/>;
    dct:rightsHolder dgn-void:IBIGroup;
    dct:subject sio:SIO_000983;
    prv:usedData dgn-void:disgenetrdf;
    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 "v2.1.0.0" .
  
  dgn-void:disgenetrdf pav:version "v2.1.0" .
}