@prefix dc: <http://purl.org/dc/terms/> .
@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP79649.RAcZdliqF7cg4HRfnDL4S04OBmFcGX36XNKULBckLBGU4> .
@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:NP79649.RAcZdliqF7cg4HRfnDL4S04OBmFcGX36XNKULBckLBGU4130_head {
  this: np:hasAssertion dgn-np:NP79649.RAcZdliqF7cg4HRfnDL4S04OBmFcGX36XNKULBckLBGU4130_assertion;
    np:hasProvenance dgn-np:NP79649.RAcZdliqF7cg4HRfnDL4S04OBmFcGX36XNKULBckLBGU4130_provenance;
    np:hasPublicationInfo dgn-np:NP79649.RAcZdliqF7cg4HRfnDL4S04OBmFcGX36XNKULBckLBGU4130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP79649.RAcZdliqF7cg4HRfnDL4S04OBmFcGX36XNKULBckLBGU4130_assertion a np:Assertion .
  
  dgn-np:NP79649.RAcZdliqF7cg4HRfnDL4S04OBmFcGX36XNKULBckLBGU4130_provenance a np:Provenance .
  
  dgn-np:NP79649.RAcZdliqF7cg4HRfnDL4S04OBmFcGX36XNKULBckLBGU4130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP79649.RAcZdliqF7cg4HRfnDL4S04OBmFcGX36XNKULBckLBGU4130_assertion {
  miriam-gene:55905 a ncit:C16612 .
  
  lld:C0030567 a ncit:C7057 .
  
  dgn-gda:DGN778d92e9762bfac5b736bf14609c2ea5 sio:SIO_000628 miriam-gene:55905, lld:C0030567;
    a sio:SIO_001122 .
}

dgn-np:NP79649.RAcZdliqF7cg4HRfnDL4S04OBmFcGX36XNKULBckLBGU4130_provenance {
  dgn-np:NP79649.RAcZdliqF7cg4HRfnDL4S04OBmFcGX36XNKULBckLBGU4130_assertion dc: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:NP79649.RAcZdliqF7cg4HRfnDL4S04OBmFcGX36XNKULBckLBGU4130_publicationInfo {
  this: dc:created "2014-10-02T12:32:39+02:00"^^xsd:dateTime;
    dc:rights <http://opendatacommons.org/licenses/odbl/1.0/>;
    dc:rightsHolder dgn-void:IBIGroup;
    dc: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" .
}