@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP53363.RAy7gyl1FEpKrnH4GR3n-DpxvnmwA1s5HxOI0roIyfJ58> .
@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:NP53363.RAy7gyl1FEpKrnH4GR3n-DpxvnmwA1s5HxOI0roIyfJ58130_head {
  this: np:hasAssertion dgn-np:NP53363.RAy7gyl1FEpKrnH4GR3n-DpxvnmwA1s5HxOI0roIyfJ58130_assertion;
    np:hasProvenance dgn-np:NP53363.RAy7gyl1FEpKrnH4GR3n-DpxvnmwA1s5HxOI0roIyfJ58130_provenance;
    np:hasPublicationInfo dgn-np:NP53363.RAy7gyl1FEpKrnH4GR3n-DpxvnmwA1s5HxOI0roIyfJ58130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP53363.RAy7gyl1FEpKrnH4GR3n-DpxvnmwA1s5HxOI0roIyfJ58130_assertion a np:Assertion .
  
  dgn-np:NP53363.RAy7gyl1FEpKrnH4GR3n-DpxvnmwA1s5HxOI0roIyfJ58130_provenance a np:Provenance .
  
  dgn-np:NP53363.RAy7gyl1FEpKrnH4GR3n-DpxvnmwA1s5HxOI0roIyfJ58130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP53363.RAy7gyl1FEpKrnH4GR3n-DpxvnmwA1s5HxOI0roIyfJ58130_assertion {
  miriam-gene:5071 a ncit:C16612 .
  
  lld:C0030567 a ncit:C7057 .
  
  dgn-gda:DGN32266d821c491e15321722d6ff40c2fd sio:SIO_000628 miriam-gene:5071, lld:C0030567;
    a sio:SIO_001122 .
}

dgn-np:NP53363.RAy7gyl1FEpKrnH4GR3n-DpxvnmwA1s5HxOI0roIyfJ58130_provenance {
  dgn-np:NP53363.RAy7gyl1FEpKrnH4GR3n-DpxvnmwA1s5HxOI0roIyfJ58130_assertion dcterms:description
      "[In order to examine the contribution of PARK2 mutations and corresponding Parkin expression in blood of North West Indian PD patients, the authors screened 120,000 patients from 2001 to 2006 for features of PD using UK Parkinson disease society brain bank clinical diagnostic criteria (UKPDBBC), and tested PARK2 mutations in 69 of those that fulfilled this criteria.]. 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:19734163;
    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:NP53363.RAy7gyl1FEpKrnH4GR3n-DpxvnmwA1s5HxOI0roIyfJ58130_publicationInfo {
  this: dcterms:created "2014-10-02T12:32:24+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" .
}