@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP58766.RAM2AXlZd6uxQGBGx3eLEAXfGvLCeVWnJecuvguMykAoo> .
@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:NP58766.RAM2AXlZd6uxQGBGx3eLEAXfGvLCeVWnJecuvguMykAoo130_head {
  this: np:hasAssertion dgn-np:NP58766.RAM2AXlZd6uxQGBGx3eLEAXfGvLCeVWnJecuvguMykAoo130_assertion;
    np:hasProvenance dgn-np:NP58766.RAM2AXlZd6uxQGBGx3eLEAXfGvLCeVWnJecuvguMykAoo130_provenance;
    np:hasPublicationInfo dgn-np:NP58766.RAM2AXlZd6uxQGBGx3eLEAXfGvLCeVWnJecuvguMykAoo130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP58766.RAM2AXlZd6uxQGBGx3eLEAXfGvLCeVWnJecuvguMykAoo130_assertion a np:Assertion .
  
  dgn-np:NP58766.RAM2AXlZd6uxQGBGx3eLEAXfGvLCeVWnJecuvguMykAoo130_provenance a np:Provenance .
  
  dgn-np:NP58766.RAM2AXlZd6uxQGBGx3eLEAXfGvLCeVWnJecuvguMykAoo130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP58766.RAM2AXlZd6uxQGBGx3eLEAXfGvLCeVWnJecuvguMykAoo130_assertion {
  miriam-gene:7166 a ncit:C16612 .
  
  lld:C1269683 a ncit:C7057 .
  
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    a sio:SIO_001122 .
}

dgn-np:NP58766.RAM2AXlZd6uxQGBGx3eLEAXfGvLCeVWnJecuvguMykAoo130_provenance {
  dgn-np:NP58766.RAM2AXlZd6uxQGBGx3eLEAXfGvLCeVWnJecuvguMykAoo130_assertion dcterms:description
      "[ The polymorphism in serotonergic system related genes may be associated with depressive symptoms in major depressive disorder. The results suggest that analysis of clusters that narrow down the phenotype may be more suitable in genetic studies of major depressive illness.]. 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:11426508;
    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:NP58766.RAM2AXlZd6uxQGBGx3eLEAXfGvLCeVWnJecuvguMykAoo130_publicationInfo {
  this: dcterms:created "2014-10-02T12:32:27+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" .
}