@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP53675.RAS6GMLkdYBucSlBaS6Yn4msHknImAvIDLqzhcWynTy7U> .
@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:NP53675.RAS6GMLkdYBucSlBaS6Yn4msHknImAvIDLqzhcWynTy7U130_head {
  this: np:hasAssertion dgn-np:NP53675.RAS6GMLkdYBucSlBaS6Yn4msHknImAvIDLqzhcWynTy7U130_assertion;
    np:hasProvenance dgn-np:NP53675.RAS6GMLkdYBucSlBaS6Yn4msHknImAvIDLqzhcWynTy7U130_provenance;
    np:hasPublicationInfo dgn-np:NP53675.RAS6GMLkdYBucSlBaS6Yn4msHknImAvIDLqzhcWynTy7U130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP53675.RAS6GMLkdYBucSlBaS6Yn4msHknImAvIDLqzhcWynTy7U130_assertion a np:Assertion .
  
  dgn-np:NP53675.RAS6GMLkdYBucSlBaS6Yn4msHknImAvIDLqzhcWynTy7U130_provenance a np:Provenance .
  
  dgn-np:NP53675.RAS6GMLkdYBucSlBaS6Yn4msHknImAvIDLqzhcWynTy7U130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP53675.RAS6GMLkdYBucSlBaS6Yn4msHknImAvIDLqzhcWynTy7U130_assertion {
  miriam-gene:1728 a ncit:C16612 .
  
  lld:C0030567 a ncit:C7057 .
  
  dgn-gda:DGNa72a59df21fb6f6901d46334d67af729 sio:SIO_000628 miriam-gene:1728, lld:C0030567;
    a sio:SIO_001122 .
}

dgn-np:NP53675.RAS6GMLkdYBucSlBaS6Yn4msHknImAvIDLqzhcWynTy7U130_provenance {
  dgn-np:NP53675.RAS6GMLkdYBucSlBaS6Yn4msHknImAvIDLqzhcWynTy7U130_assertion dcterms:description
      "[ This study revealed significant differences in genotypic frequencies between PD group and control group. The findings supported the hypothesis about an association between NQO1 gene and PD, suggesting that the age at onset of PD might be related to the putative association, and NQO1 cDNA C609T site be a risk factor for PD.]. 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:15079792;
    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:NP53675.RAS6GMLkdYBucSlBaS6Yn4msHknImAvIDLqzhcWynTy7U130_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>,
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    pav:createdBy <http://orcid.org/0000-0003-0169-8159>;
    pav:version "v2.1.0.0" .
  
  dgn-void:disgenetrdf pav:version "v2.1.0" .
}