@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP53605.RApXA6R71X21QQqFgoinluhbzKqDA_-eIM73rCysE9EUg> .
@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:NP53605.RApXA6R71X21QQqFgoinluhbzKqDA_-eIM73rCysE9EUg130_head {
  this: np:hasAssertion dgn-np:NP53605.RApXA6R71X21QQqFgoinluhbzKqDA_-eIM73rCysE9EUg130_assertion;
    np:hasProvenance dgn-np:NP53605.RApXA6R71X21QQqFgoinluhbzKqDA_-eIM73rCysE9EUg130_provenance;
    np:hasPublicationInfo dgn-np:NP53605.RApXA6R71X21QQqFgoinluhbzKqDA_-eIM73rCysE9EUg130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP53605.RApXA6R71X21QQqFgoinluhbzKqDA_-eIM73rCysE9EUg130_assertion a np:Assertion .
  
  dgn-np:NP53605.RApXA6R71X21QQqFgoinluhbzKqDA_-eIM73rCysE9EUg130_provenance a np:Provenance .
  
  dgn-np:NP53605.RApXA6R71X21QQqFgoinluhbzKqDA_-eIM73rCysE9EUg130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP53605.RApXA6R71X21QQqFgoinluhbzKqDA_-eIM73rCysE9EUg130_assertion {
  miriam-gene:4929 a ncit:C16612 .
  
  lld:C0030567 a ncit:C7057 .
  
  dgn-gda:DGN45a9149522a3bde041ef3c7687938c08 sio:SIO_000628 miriam-gene:4929, lld:C0030567;
    a sio:SIO_001122 .
}

dgn-np:NP53605.RApXA6R71X21QQqFgoinluhbzKqDA_-eIM73rCysE9EUg130_provenance {
  dgn-np:NP53605.RApXA6R71X21QQqFgoinluhbzKqDA_-eIM73rCysE9EUg130_assertion dcterms:description
      "[Our results failed to replicate the association initially observed and none of the mutations were present in our familial Parkinson's disease cases. These observations suggest that this gene is unlikely to play a major effect in French familial Parkinson 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:15276233;
    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:NP53605.RApXA6R71X21QQqFgoinluhbzKqDA_-eIM73rCysE9EUg130_publicationInfo {
  this: dcterms:created "2014-10-02T12:32:25+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" .
}