@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP62748.RA1FfUt4wbrnR7WlEdkXftm99wRXnMabKhStAhD21DN6M> .
@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:NP62748.RA1FfUt4wbrnR7WlEdkXftm99wRXnMabKhStAhD21DN6M130_head {
  this: np:hasAssertion dgn-np:NP62748.RA1FfUt4wbrnR7WlEdkXftm99wRXnMabKhStAhD21DN6M130_assertion;
    np:hasProvenance dgn-np:NP62748.RA1FfUt4wbrnR7WlEdkXftm99wRXnMabKhStAhD21DN6M130_provenance;
    np:hasPublicationInfo dgn-np:NP62748.RA1FfUt4wbrnR7WlEdkXftm99wRXnMabKhStAhD21DN6M130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP62748.RA1FfUt4wbrnR7WlEdkXftm99wRXnMabKhStAhD21DN6M130_assertion a np:Assertion .
  
  dgn-np:NP62748.RA1FfUt4wbrnR7WlEdkXftm99wRXnMabKhStAhD21DN6M130_provenance a np:Provenance .
  
  dgn-np:NP62748.RA1FfUt4wbrnR7WlEdkXftm99wRXnMabKhStAhD21DN6M130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP62748.RA1FfUt4wbrnR7WlEdkXftm99wRXnMabKhStAhD21DN6M130_assertion {
  miriam-gene:1312 a ncit:C16612 .
  
  lld:C0011570 a ncit:C7057 .
  
  dgn-gda:DGN027b7f75bf581f54d4f15253bfff4747 sio:SIO_000628 miriam-gene:1312, lld:C0011570;
    a sio:SIO_001122 .
}

dgn-np:NP62748.RA1FfUt4wbrnR7WlEdkXftm99wRXnMabKhStAhD21DN6M130_provenance {
  dgn-np:NP62748.RA1FfUt4wbrnR7WlEdkXftm99wRXnMabKhStAhD21DN6M130_assertion dcterms:description
      "[In summary, the present study supports a potentially gender-specific significant impact of COMT gene variation on electroconvulsive therapy response, with COMT 158val risk allele carriers suffering from more severe, pharmacologically less efficiently treatable depression and thus possibly deriving greater benefit from ECT in the first place.]. 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:19309019;
    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:NP62748.RA1FfUt4wbrnR7WlEdkXftm99wRXnMabKhStAhD21DN6M130_publicationInfo {
  this: dcterms:created "2014-10-02T12:32:29+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" .
}