@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP51554.RAbIeCJZ-LGdfvt6yd_H4So9bSFnRDnN5spZ3S_pbLNms> .
@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:NP51554.RAbIeCJZ-LGdfvt6yd_H4So9bSFnRDnN5spZ3S_pbLNms130_head {
  this: np:hasAssertion dgn-np:NP51554.RAbIeCJZ-LGdfvt6yd_H4So9bSFnRDnN5spZ3S_pbLNms130_assertion;
    np:hasProvenance dgn-np:NP51554.RAbIeCJZ-LGdfvt6yd_H4So9bSFnRDnN5spZ3S_pbLNms130_provenance;
    np:hasPublicationInfo dgn-np:NP51554.RAbIeCJZ-LGdfvt6yd_H4So9bSFnRDnN5spZ3S_pbLNms130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP51554.RAbIeCJZ-LGdfvt6yd_H4So9bSFnRDnN5spZ3S_pbLNms130_assertion a np:Assertion .
  
  dgn-np:NP51554.RAbIeCJZ-LGdfvt6yd_H4So9bSFnRDnN5spZ3S_pbLNms130_provenance a np:Provenance .
  
  dgn-np:NP51554.RAbIeCJZ-LGdfvt6yd_H4So9bSFnRDnN5spZ3S_pbLNms130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP51554.RAbIeCJZ-LGdfvt6yd_H4So9bSFnRDnN5spZ3S_pbLNms130_assertion {
  miriam-gene:6531 a ncit:C16612 .
  
  lld:C0030567 a ncit:C7057 .
  
  dgn-gda:DGN806f1a8d617c73e43ee0333d6c63c813 sio:SIO_000628 miriam-gene:6531, lld:C0030567;
    a sio:SIO_001122 .
}

dgn-np:NP51554.RAbIeCJZ-LGdfvt6yd_H4So9bSFnRDnN5spZ3S_pbLNms130_provenance {
  dgn-np:NP51554.RAbIeCJZ-LGdfvt6yd_H4So9bSFnRDnN5spZ3S_pbLNms130_assertion dcterms:description
      "[The findings not only support an association between DAT gene and PD but also suggest the relationship of the 3'VNTR polymorphism of DAT gene with the age at the onset of 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:11774209;
    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:NP51554.RAbIeCJZ-LGdfvt6yd_H4So9bSFnRDnN5spZ3S_pbLNms130_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" .
}