@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP643757.RAcsP3gluFri2s_fKcGwh14qx0uoSUt4uDhnQNMOn_osA> .
@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:NP643757.RAcsP3gluFri2s_fKcGwh14qx0uoSUt4uDhnQNMOn_osA130_head {
  this: np:hasAssertion dgn-np:NP643757.RAcsP3gluFri2s_fKcGwh14qx0uoSUt4uDhnQNMOn_osA130_assertion ;
    np:hasProvenance dgn-np:NP643757.RAcsP3gluFri2s_fKcGwh14qx0uoSUt4uDhnQNMOn_osA130_provenance ;
    np:hasPublicationInfo dgn-np:NP643757.RAcsP3gluFri2s_fKcGwh14qx0uoSUt4uDhnQNMOn_osA130_publicationInfo ;
    a np:Nanopublication .
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  dgn-np:NP643757.RAcsP3gluFri2s_fKcGwh14qx0uoSUt4uDhnQNMOn_osA130_provenance a np:Provenance .
  dgn-np:NP643757.RAcsP3gluFri2s_fKcGwh14qx0uoSUt4uDhnQNMOn_osA130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP643757.RAcsP3gluFri2s_fKcGwh14qx0uoSUt4uDhnQNMOn_osA130_assertion {
  miriam-gene:79947 a ncit:C16612 .
  lld:C1263846 a ncit:C7057 .
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}
dgn-np:NP643757.RAcsP3gluFri2s_fKcGwh14qx0uoSUt4uDhnQNMOn_osA130_provenance {
  dgn-np:NP643757.RAcsP3gluFri2s_fKcGwh14qx0uoSUt4uDhnQNMOn_osA130_assertion dcterms:description "[The aims of this study were to examine the association of the ADRA2A MspI and DraI polymorphisms with ADHD in Korean subjects, and to determine the relationship between the genotypes of these two polymorphisms and the candidate endophenotypes, as measured by the continuous performance test (CPT).]. 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:18314873 ;
    prov:wasDerivedFrom dgn-void:befree-20140225 ;
    prov:wasGeneratedBy eco:ECO_0000203 .
  dgn-void:befree-20140225 pav:importedOn "2014-02-25"^^xsd:date .
  dgn-void:source_evidence_literature a eco:ECO_0000212 ;
    rdfs:comment "Gene-disease associations inferred from text-mining the literature."@en ;
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}
dgn-np:NP643757.RAcsP3gluFri2s_fKcGwh14qx0uoSUt4uDhnQNMOn_osA130_publicationInfo {
  this: dcterms:created "2014-10-02T12:38:28+02:00"^^xsd:dateTime ;
    dcterms:rights <http://opendatacommons.org/licenses/odbl/1.0/> ;
    dcterms:rightsHolder dgn-void:IBIGroup ;
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    prv:usedData dgn-void:disgenetrdf ;
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}