@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP766591.RA4T2tduI3qH0ri_LmS4CBNw4iywsNkbjsIXqQ5ehH6Bc> .
@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:NP766591.RA4T2tduI3qH0ri_LmS4CBNw4iywsNkbjsIXqQ5ehH6Bc130_head {
  this: np:hasAssertion dgn-np:NP766591.RA4T2tduI3qH0ri_LmS4CBNw4iywsNkbjsIXqQ5ehH6Bc130_assertion;
    np:hasProvenance dgn-np:NP766591.RA4T2tduI3qH0ri_LmS4CBNw4iywsNkbjsIXqQ5ehH6Bc130_provenance;
    np:hasPublicationInfo dgn-np:NP766591.RA4T2tduI3qH0ri_LmS4CBNw4iywsNkbjsIXqQ5ehH6Bc130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP766591.RA4T2tduI3qH0ri_LmS4CBNw4iywsNkbjsIXqQ5ehH6Bc130_assertion a np:Assertion .
  
  dgn-np:NP766591.RA4T2tduI3qH0ri_LmS4CBNw4iywsNkbjsIXqQ5ehH6Bc130_provenance a np:Provenance .
  
  dgn-np:NP766591.RA4T2tduI3qH0ri_LmS4CBNw4iywsNkbjsIXqQ5ehH6Bc130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP766591.RA4T2tduI3qH0ri_LmS4CBNw4iywsNkbjsIXqQ5ehH6Bc130_assertion {
  miriam-gene:4524 a ncit:C16612 .
  
  lld:C0524620 a ncit:C7057 .
  
  dgn-gda:DGN3e9c865e4497e415f7f03b4b512f270c sio:SIO_000628 miriam-gene:4524, lld:C0524620;
    a sio:SIO_001121 .
}

dgn-np:NP766591.RA4T2tduI3qH0ri_LmS4CBNw4iywsNkbjsIXqQ5ehH6Bc130_provenance {
  dgn-np:NP766591.RA4T2tduI3qH0ri_LmS4CBNw4iywsNkbjsIXqQ5ehH6Bc130_assertion dcterms:description
      "[We found that genotype Met/Met of the Val66Met polymorphism of the brain-derived neurotrophic factor gene was positively associated with depressive disorder (P < 0.05), but we were not able to find any significant associations of both the depressive disorder and metabolic syndrome with the remaining polymorphisms studied (methylenetetrahydrofolate reductase 677CT, methylenetet rahydrofolate reductase 1298AC, endothelial nitric oxide synthase Glu298Asp, and tyrosine hydroxylase).]. 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:20163778;
    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:NP766591.RA4T2tduI3qH0ri_LmS4CBNw4iywsNkbjsIXqQ5ehH6Bc130_publicationInfo {
  this: dcterms:created "2014-10-02T12:39:44+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" .
}