@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP190987.RACsEUYf2ui6XtO-DdmEA0FUjfWHEswSJH3E9PfPjtiDY> .
@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:NP190987.RACsEUYf2ui6XtO-DdmEA0FUjfWHEswSJH3E9PfPjtiDY130_head {
  this: np:hasAssertion dgn-np:NP190987.RACsEUYf2ui6XtO-DdmEA0FUjfWHEswSJH3E9PfPjtiDY130_assertion;
    np:hasProvenance dgn-np:NP190987.RACsEUYf2ui6XtO-DdmEA0FUjfWHEswSJH3E9PfPjtiDY130_provenance;
    np:hasPublicationInfo dgn-np:NP190987.RACsEUYf2ui6XtO-DdmEA0FUjfWHEswSJH3E9PfPjtiDY130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP190987.RACsEUYf2ui6XtO-DdmEA0FUjfWHEswSJH3E9PfPjtiDY130_assertion a np:Assertion .
  
  dgn-np:NP190987.RACsEUYf2ui6XtO-DdmEA0FUjfWHEswSJH3E9PfPjtiDY130_provenance a np:Provenance .
  
  dgn-np:NP190987.RACsEUYf2ui6XtO-DdmEA0FUjfWHEswSJH3E9PfPjtiDY130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP190987.RACsEUYf2ui6XtO-DdmEA0FUjfWHEswSJH3E9PfPjtiDY130_assertion {
  miriam-gene:3359 a ncit:C16612 .
  
  lld:C1970943 a ncit:C7057 .
  
  dgn-gda:DGNbe7eb1172d4f1ad5f348890745815836 sio:SIO_000628 miriam-gene:3359, lld:C1970943;
    a sio:SIO_001121 .
}

dgn-np:NP190987.RACsEUYf2ui6XtO-DdmEA0FUjfWHEswSJH3E9PfPjtiDY130_provenance {
  dgn-np:NP190987.RACsEUYf2ui6XtO-DdmEA0FUjfWHEswSJH3E9PfPjtiDY130_assertion dcterms:description
      "[Three single nucleotide polymorphisms (SNPs) in the HTR3A and HTR3B genes (rs1062613, rs1176744 and rs3831455) have been associated with bipolar affective disorder (BPAD) in pilot studies, and all of them are of functional relevance.]. 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:22832903;
    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:NP190987.RACsEUYf2ui6XtO-DdmEA0FUjfWHEswSJH3E9PfPjtiDY130_publicationInfo {
  this: dcterms:created "2014-10-02T12:33:45+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" .
}