@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP43321.RA0RiJoDTlc1qwadwlZnhP07Wc-O2MmSHdPL_RN01mVzo> .
@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:NP43321.RA0RiJoDTlc1qwadwlZnhP07Wc-O2MmSHdPL_RN01mVzo130_head {
  this: np:hasAssertion dgn-np:NP43321.RA0RiJoDTlc1qwadwlZnhP07Wc-O2MmSHdPL_RN01mVzo130_assertion;
    np:hasProvenance dgn-np:NP43321.RA0RiJoDTlc1qwadwlZnhP07Wc-O2MmSHdPL_RN01mVzo130_provenance;
    np:hasPublicationInfo dgn-np:NP43321.RA0RiJoDTlc1qwadwlZnhP07Wc-O2MmSHdPL_RN01mVzo130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP43321.RA0RiJoDTlc1qwadwlZnhP07Wc-O2MmSHdPL_RN01mVzo130_assertion a np:Assertion .
  
  dgn-np:NP43321.RA0RiJoDTlc1qwadwlZnhP07Wc-O2MmSHdPL_RN01mVzo130_provenance a np:Provenance .
  
  dgn-np:NP43321.RA0RiJoDTlc1qwadwlZnhP07Wc-O2MmSHdPL_RN01mVzo130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP43321.RA0RiJoDTlc1qwadwlZnhP07Wc-O2MmSHdPL_RN01mVzo130_assertion {
  miriam-gene:2932 a ncit:C16612 .
  
  lld:C0005586 a ncit:C7057 .
  
  dgn-gda:DGN6ba65c5bc98650d5f78cfc81ea23ab32 sio:SIO_000628 miriam-gene:2932, lld:C0005586;
    a sio:SIO_001122 .
}

dgn-np:NP43321.RA0RiJoDTlc1qwadwlZnhP07Wc-O2MmSHdPL_RN01mVzo130_provenance {
  dgn-np:NP43321.RA0RiJoDTlc1qwadwlZnhP07Wc-O2MmSHdPL_RN01mVzo130_assertion dcterms:description
      "[Overall, these observations suggest a protective role for this genotype in respect to bipolar illness. Results warrant interest for the variants of genes pertaining to the molecular clock as possible endophenotypes of bipolar disorder, and for GSK3-beta as a target of a new class of antidepressant drugs, but caution ought to be taken in interpreting these preliminary results and future replication studies must be awaited because of the low frequency of the GSK3-beta*C/C genotype in the studied populations.]. 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:15351432;
    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:NP43321.RA0RiJoDTlc1qwadwlZnhP07Wc-O2MmSHdPL_RN01mVzo130_publicationInfo {
  this: dcterms:created "2014-10-02T12:32:19+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" .
}