@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP514419.RAbveyqRIMKUsDqgQNTpFtytHOVWrHHQPeWd_4alHd0ms> .
@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:NP514419.RAbveyqRIMKUsDqgQNTpFtytHOVWrHHQPeWd_4alHd0ms130_head {
  this: np:hasAssertion dgn-np:NP514419.RAbveyqRIMKUsDqgQNTpFtytHOVWrHHQPeWd_4alHd0ms130_assertion ;
    np:hasProvenance dgn-np:NP514419.RAbveyqRIMKUsDqgQNTpFtytHOVWrHHQPeWd_4alHd0ms130_provenance ;
    np:hasPublicationInfo dgn-np:NP514419.RAbveyqRIMKUsDqgQNTpFtytHOVWrHHQPeWd_4alHd0ms130_publicationInfo ;
    a np:Nanopublication .
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}
dgn-np:NP514419.RAbveyqRIMKUsDqgQNTpFtytHOVWrHHQPeWd_4alHd0ms130_assertion {
  miriam-gene:121278 a ncit:C16612 .
  lld:C1269683 a ncit:C7057 .
  dgn-gda:DGN375fe176a054e624475757a17360b1b6 sio:SIO_000628 miriam-gene:121278 , lld:C1269683 ;
    a sio:SIO_001121 .
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dgn-np:NP514419.RAbveyqRIMKUsDqgQNTpFtytHOVWrHHQPeWd_4alHd0ms130_provenance {
  dgn-np:NP514419.RAbveyqRIMKUsDqgQNTpFtytHOVWrHHQPeWd_4alHd0ms130_assertion dcterms:description "[The three genes, namely, tryptophan hydroxylase 2 (TPH2), kynurenine 3 monooxygenase (KMO) and kynurenine amino transferase 3 (KAT III) SNPs and haplotype association analysis was performed in 338 (266 major depression and 72 bipolar depression) unrelated Caucasian patients with major depressive episodes and 310 age, gender and ethnicity matched controls.]. 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 ;
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}
dgn-np:NP514419.RAbveyqRIMKUsDqgQNTpFtytHOVWrHHQPeWd_4alHd0ms130_publicationInfo {
  this: dcterms:created "2014-10-02T12:37:06+02:00"^^xsd:dateTime ;
    dcterms:rights <http://opendatacommons.org/licenses/odbl/1.0/> ;
    dcterms:rightsHolder dgn-void:IBIGroup ;
    dcterms:subject sio:SIO_000983 ;
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