@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP157782.RACl8Cjj5wepTtUzjEco0L1clW8vvNb5-49U2tsactR2s> .
@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:NP157782.RACl8Cjj5wepTtUzjEco0L1clW8vvNb5-49U2tsactR2s130_head {
  this: np:hasAssertion dgn-np:NP157782.RACl8Cjj5wepTtUzjEco0L1clW8vvNb5-49U2tsactR2s130_assertion;
    np:hasProvenance dgn-np:NP157782.RACl8Cjj5wepTtUzjEco0L1clW8vvNb5-49U2tsactR2s130_provenance;
    np:hasPublicationInfo dgn-np:NP157782.RACl8Cjj5wepTtUzjEco0L1clW8vvNb5-49U2tsactR2s130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP157782.RACl8Cjj5wepTtUzjEco0L1clW8vvNb5-49U2tsactR2s130_assertion a np:Assertion .
  
  dgn-np:NP157782.RACl8Cjj5wepTtUzjEco0L1clW8vvNb5-49U2tsactR2s130_provenance a np:Provenance .
  
  dgn-np:NP157782.RACl8Cjj5wepTtUzjEco0L1clW8vvNb5-49U2tsactR2s130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP157782.RACl8Cjj5wepTtUzjEco0L1clW8vvNb5-49U2tsactR2s130_assertion {
  miriam-gene:4128 a ncit:C16612 .
  
  lld:C1263846 a ncit:C7057 .
  
  dgn-gda:DGN3327cd71438e07b7577cb25a8d2f28f5 sio:SIO_000628 miriam-gene:4128, lld:C1263846;
    a sio:SIO_001121 .
}

dgn-np:NP157782.RACl8Cjj5wepTtUzjEco0L1clW8vvNb5-49U2tsactR2s130_provenance {
  dgn-np:NP157782.RACl8Cjj5wepTtUzjEco0L1clW8vvNb5-49U2tsactR2s130_assertion dcterms:description
      "[Since our previous association studies between attention deficit hyperactivity disorder (ADHD) and these two functional polymorphisms consistently showed the low activity alleles were preferentially transmitted to inattentive ADHD boys, the goal of the present study was to test the hypothesis that the interaction between COMT Val158Met and MAOA-uVNTR may affect the intelligence in a clinical sample of Chinese male ADHD subjects (n = 264).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en;
    wi:evidence dgn-void:source_evidence_literature;
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    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;
    rdfs:label "DisGeNET evidence - LITERATURE"@en .
}

dgn-np:NP157782.RACl8Cjj5wepTtUzjEco0L1clW8vvNb5-49U2tsactR2s130_publicationInfo {
  this: dcterms:created "2014-10-02T12:33:25+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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  dgn-void:disgenetrdf pav:version "v2.1.0" .
}