@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP86467.RAZhZVs3QJqou3a6zrt2Y-aCAy4aC5O6vKQ83CMde7JOo> .
@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:NP86467.RAZhZVs3QJqou3a6zrt2Y-aCAy4aC5O6vKQ83CMde7JOo130_head {
  this: np:hasAssertion dgn-np:NP86467.RAZhZVs3QJqou3a6zrt2Y-aCAy4aC5O6vKQ83CMde7JOo130_assertion ;
    np:hasProvenance dgn-np:NP86467.RAZhZVs3QJqou3a6zrt2Y-aCAy4aC5O6vKQ83CMde7JOo130_provenance ;
    np:hasPublicationInfo dgn-np:NP86467.RAZhZVs3QJqou3a6zrt2Y-aCAy4aC5O6vKQ83CMde7JOo130_publicationInfo ;
    a np:Nanopublication .
  dgn-np:NP86467.RAZhZVs3QJqou3a6zrt2Y-aCAy4aC5O6vKQ83CMde7JOo130_assertion a np:Assertion .
  dgn-np:NP86467.RAZhZVs3QJqou3a6zrt2Y-aCAy4aC5O6vKQ83CMde7JOo130_provenance a np:Provenance .
  dgn-np:NP86467.RAZhZVs3QJqou3a6zrt2Y-aCAy4aC5O6vKQ83CMde7JOo130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP86467.RAZhZVs3QJqou3a6zrt2Y-aCAy4aC5O6vKQ83CMde7JOo130_assertion {
  miriam-gene:3359 a ncit:C16612 .
  lld:C0011570 a ncit:C7057 .
  dgn-gda:DGNb50d8553e52b82fad9fe6d839dbf20dc sio:SIO_000628 miriam-gene:3359 , lld:C0011570 ;
    a sio:SIO_001122 .
}
dgn-np:NP86467.RAZhZVs3QJqou3a6zrt2Y-aCAy4aC5O6vKQ83CMde7JOo130_provenance {
  dgn-np:NP86467.RAZhZVs3QJqou3a6zrt2Y-aCAy4aC5O6vKQ83CMde7JOo130_assertion dcterms:description "[These findings suggest that the HTR3A CC genotype may be associated with alterations in brain structures central to emotion processing, particularly when exposed to stress, and further highlight the potential role of the serotonin system in the pathophysiology of affective disorders. In contrast, those individuals with the T allele, in particular the TT genotype, may be more protected from such alterations combined with minimal exposure to ELS events.]. 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:20694966 ;
    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:NP86467.RAZhZVs3QJqou3a6zrt2Y-aCAy4aC5O6vKQ83CMde7JOo130_publicationInfo {
  this: dcterms:created "2014-10-02T12:32:42+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" .
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}