@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP168144.RAIKDYVcfDvKvbr79tSuPUMs25wAn2ss6F6QBQ1wqoAlk> .
@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:NP168144.RAIKDYVcfDvKvbr79tSuPUMs25wAn2ss6F6QBQ1wqoAlk130_head {
  this: np:hasAssertion dgn-np:NP168144.RAIKDYVcfDvKvbr79tSuPUMs25wAn2ss6F6QBQ1wqoAlk130_assertion;
    np:hasProvenance dgn-np:NP168144.RAIKDYVcfDvKvbr79tSuPUMs25wAn2ss6F6QBQ1wqoAlk130_provenance;
    np:hasPublicationInfo dgn-np:NP168144.RAIKDYVcfDvKvbr79tSuPUMs25wAn2ss6F6QBQ1wqoAlk130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP168144.RAIKDYVcfDvKvbr79tSuPUMs25wAn2ss6F6QBQ1wqoAlk130_assertion a np:Assertion .
  
  dgn-np:NP168144.RAIKDYVcfDvKvbr79tSuPUMs25wAn2ss6F6QBQ1wqoAlk130_provenance a np:Provenance .
  
  dgn-np:NP168144.RAIKDYVcfDvKvbr79tSuPUMs25wAn2ss6F6QBQ1wqoAlk130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP168144.RAIKDYVcfDvKvbr79tSuPUMs25wAn2ss6F6QBQ1wqoAlk130_assertion {
  miriam-gene:2784 a ncit:C16612 .
  
  lld:C1269683 a ncit:C7057 .
  
  dgn-gda:DGN3ee0d31a62338207e5238f0614068cd9 sio:SIO_000628 miriam-gene:2784, lld:C1269683;
    a sio:SIO_001121 .
}

dgn-np:NP168144.RAIKDYVcfDvKvbr79tSuPUMs25wAn2ss6F6QBQ1wqoAlk130_provenance {
  dgn-np:NP168144.RAIKDYVcfDvKvbr79tSuPUMs25wAn2ss6F6QBQ1wqoAlk130_assertion dcterms:description
      "[Although the C825T polymorphism of the GNB3 gene may affect the pathogenesis of MDD, our results do not support the hypothesis that this polymorphism is involved in the therapeutic response to mirtazapine in Korean patients with MDD.]. 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:17943025;
    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:NP168144.RAIKDYVcfDvKvbr79tSuPUMs25wAn2ss6F6QBQ1wqoAlk130_publicationInfo {
  this: dcterms:created "2014-10-02T12:33:31+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" .
}