@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP594646.RAvG_jg2B725OuCbrYRDcP3nm003IcJoFiO5DRs_t67ws> .
@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:NP594646.RAvG_jg2B725OuCbrYRDcP3nm003IcJoFiO5DRs_t67ws130_head {
  this: np:hasAssertion dgn-np:NP594646.RAvG_jg2B725OuCbrYRDcP3nm003IcJoFiO5DRs_t67ws130_assertion;
    np:hasProvenance dgn-np:NP594646.RAvG_jg2B725OuCbrYRDcP3nm003IcJoFiO5DRs_t67ws130_provenance;
    np:hasPublicationInfo dgn-np:NP594646.RAvG_jg2B725OuCbrYRDcP3nm003IcJoFiO5DRs_t67ws130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP594646.RAvG_jg2B725OuCbrYRDcP3nm003IcJoFiO5DRs_t67ws130_assertion a np:Assertion .
  
  dgn-np:NP594646.RAvG_jg2B725OuCbrYRDcP3nm003IcJoFiO5DRs_t67ws130_provenance a np:Provenance .
  
  dgn-np:NP594646.RAvG_jg2B725OuCbrYRDcP3nm003IcJoFiO5DRs_t67ws130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP594646.RAvG_jg2B725OuCbrYRDcP3nm003IcJoFiO5DRs_t67ws130_assertion {
  miriam-gene:6999 a ncit:C16612 .
  
  lld:C0497327 a ncit:C7057 .
  
  dgn-gda:DGNa8de5ecb1a352607bd2c2e9fecc5a6c4 sio:SIO_000628 miriam-gene:6999, lld:C0497327;
    a sio:SIO_001121 .
}

dgn-np:NP594646.RAvG_jg2B725OuCbrYRDcP3nm003IcJoFiO5DRs_t67ws130_provenance {
  dgn-np:NP594646.RAvG_jg2B725OuCbrYRDcP3nm003IcJoFiO5DRs_t67ws130_assertion dcterms:description
      "[A prospective, longitudinal study was set up to investigate possible genetic associations of behavioral and psychological signs and symptoms of dementia (BPSD) in Alzheimer's disease (AD) with two candidate genes in the serotonergic neurotransmitter pathway: serotonin transporter (SLC6A4) and brain-specific tryptophan hydroxylase (TPH2).]. 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:23334703;
    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:NP594646.RAvG_jg2B725OuCbrYRDcP3nm003IcJoFiO5DRs_t67ws130_publicationInfo {
  this: dcterms:created "2014-10-02T12:37:57+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" .
}