@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP271364.RABjpK9xM_GtPuwHemHiThidxscJJWULgjzgtRQKKU_qQ> .
@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:NP271364.RABjpK9xM_GtPuwHemHiThidxscJJWULgjzgtRQKKU_qQ130_head {
  this: np:hasAssertion dgn-np:NP271364.RABjpK9xM_GtPuwHemHiThidxscJJWULgjzgtRQKKU_qQ130_assertion;
    np:hasProvenance dgn-np:NP271364.RABjpK9xM_GtPuwHemHiThidxscJJWULgjzgtRQKKU_qQ130_provenance;
    np:hasPublicationInfo dgn-np:NP271364.RABjpK9xM_GtPuwHemHiThidxscJJWULgjzgtRQKKU_qQ130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP271364.RABjpK9xM_GtPuwHemHiThidxscJJWULgjzgtRQKKU_qQ130_assertion a np:Assertion .
  
  dgn-np:NP271364.RABjpK9xM_GtPuwHemHiThidxscJJWULgjzgtRQKKU_qQ130_provenance a np:Provenance .
  
  dgn-np:NP271364.RABjpK9xM_GtPuwHemHiThidxscJJWULgjzgtRQKKU_qQ130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP271364.RABjpK9xM_GtPuwHemHiThidxscJJWULgjzgtRQKKU_qQ130_assertion {
  miriam-gene:6532 a ncit:C16612 .
  
  lld:C1842981 a ncit:C7057 .
  
  dgn-gda:DGN430fcd3f47715ef59f23ac402fdccf73 sio:SIO_000628 miriam-gene:6532, lld:C1842981;
    a sio:SIO_001121 .
}

dgn-np:NP271364.RABjpK9xM_GtPuwHemHiThidxscJJWULgjzgtRQKKU_qQ130_provenance {
  dgn-np:NP271364.RABjpK9xM_GtPuwHemHiThidxscJJWULgjzgtRQKKU_qQ130_assertion dcterms:description
      "[A functional polymorphism in the promoter region of the human serotonin transporter gene (SLC6A4) has been associated with several dimensions of neuroticism and psychopathology, especially anxiety traits, but the predictive value of this genotype against these complex behaviors has been inconsistent.]. 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:12130784;
    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:NP271364.RABjpK9xM_GtPuwHemHiThidxscJJWULgjzgtRQKKU_qQ130_publicationInfo {
  this: dcterms:created "2014-10-02T12:34:31+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" .
}