@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP54978.RAiQgrJ0ud30Hk1UkF_ISCGwZCJHgdZhDmBmqaARV1ONg> .
@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:NP54978.RAiQgrJ0ud30Hk1UkF_ISCGwZCJHgdZhDmBmqaARV1ONg130_head {
  this: np:hasAssertion dgn-np:NP54978.RAiQgrJ0ud30Hk1UkF_ISCGwZCJHgdZhDmBmqaARV1ONg130_assertion;
    np:hasProvenance dgn-np:NP54978.RAiQgrJ0ud30Hk1UkF_ISCGwZCJHgdZhDmBmqaARV1ONg130_provenance;
    np:hasPublicationInfo dgn-np:NP54978.RAiQgrJ0ud30Hk1UkF_ISCGwZCJHgdZhDmBmqaARV1ONg130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP54978.RAiQgrJ0ud30Hk1UkF_ISCGwZCJHgdZhDmBmqaARV1ONg130_assertion a np:Assertion .
  
  dgn-np:NP54978.RAiQgrJ0ud30Hk1UkF_ISCGwZCJHgdZhDmBmqaARV1ONg130_provenance a np:Provenance .
  
  dgn-np:NP54978.RAiQgrJ0ud30Hk1UkF_ISCGwZCJHgdZhDmBmqaARV1ONg130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP54978.RAiQgrJ0ud30Hk1UkF_ISCGwZCJHgdZhDmBmqaARV1ONg130_assertion {
  miriam-gene:4128 a ncit:C16612 .
  
  lld:C1842981 a ncit:C7057 .
  
  dgn-gda:DGN9f84f8391818d95192837f816365a077 sio:SIO_000628 miriam-gene:4128, lld:C1842981;
    a sio:SIO_001122 .
}

dgn-np:NP54978.RAiQgrJ0ud30Hk1UkF_ISCGwZCJHgdZhDmBmqaARV1ONg130_provenance {
  dgn-np:NP54978.RAiQgrJ0ud30Hk1UkF_ISCGwZCJHgdZhDmBmqaARV1ONg130_assertion dcterms:description
      "[We found weak evidence for association with COMT genotype, when the females and males were considered separately, and for MAOA genotype in males only. There was no significant interaction between COMT and MAOA.]. 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:12815746;
    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:NP54978.RAiQgrJ0ud30Hk1UkF_ISCGwZCJHgdZhDmBmqaARV1ONg130_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>,
      <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" .
}