@prefix dct: <http://purl.org/dc/terms/> .
@prefix orcid: <http://orcid.org/> .
@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP59893.RAy4negiyR-kHldGmpo3ZR_nfHYBy7ObauxzmfDtAXk8o> .
@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 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:NP59893.RAy4negiyR-kHldGmpo3ZR_nfHYBy7ObauxzmfDtAXk8o130_head {
  this: np:hasAssertion dgn-np:NP59893.RAy4negiyR-kHldGmpo3ZR_nfHYBy7ObauxzmfDtAXk8o130_assertion;
    np:hasProvenance dgn-np:NP59893.RAy4negiyR-kHldGmpo3ZR_nfHYBy7ObauxzmfDtAXk8o130_provenance;
    np:hasPublicationInfo dgn-np:NP59893.RAy4negiyR-kHldGmpo3ZR_nfHYBy7ObauxzmfDtAXk8o130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP59893.RAy4negiyR-kHldGmpo3ZR_nfHYBy7ObauxzmfDtAXk8o130_assertion a np:Assertion .
  
  dgn-np:NP59893.RAy4negiyR-kHldGmpo3ZR_nfHYBy7ObauxzmfDtAXk8o130_provenance a np:Provenance .
  
  dgn-np:NP59893.RAy4negiyR-kHldGmpo3ZR_nfHYBy7ObauxzmfDtAXk8o130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP59893.RAy4negiyR-kHldGmpo3ZR_nfHYBy7ObauxzmfDtAXk8o130_assertion {
  miriam-gene:1312 a ncit:C16612 .
  
  lld:C1263846 a ncit:C7057 .
  
  dgn-gda:DGN5e2dcfa1f18738258945aba8b3e8b473 sio:SIO_000628 miriam-gene:1312, lld:C1263846;
    a sio:SIO_001122 .
}

dgn-np:NP59893.RAy4negiyR-kHldGmpo3ZR_nfHYBy7ObauxzmfDtAXk8o130_provenance {
  dgn-np:NP59893.RAy4negiyR-kHldGmpo3ZR_nfHYBy7ObauxzmfDtAXk8o130_assertion dct:description
      "[do not support the hypothesis that common variants in the SLC6A2 and COMT genes in particular are associated with ADHD, but might give some evidence for interactive effects between these gene variants on ADHD severity.]. 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:17994190;
    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:NP59893.RAy4negiyR-kHldGmpo3ZR_nfHYBy7ObauxzmfDtAXk8o130_publicationInfo {
  this: dct:created "2014-10-02T12:32:28+02:00"^^xsd:dateTime;
    dct:rights <http://opendatacommons.org/licenses/odbl/1.0/>;
    dct:rightsHolder dgn-void:IBIGroup;
    dct:subject sio:SIO_000983;
    prv:usedData dgn-void:disgenetrdf;
    pav:authoredBy orcid:0000-0001-5999-6269, orcid:0000-0002-7534-7661, orcid:0000-0002-9383-528X,
      orcid:0000-0003-0169-8159, orcid:0000-0003-1244-7654;
    pav:createdBy orcid:0000-0003-0169-8159;
    pav:version "v2.1.0.0" .
  
  dgn-void:disgenetrdf pav:version "v2.1.0" .
}