@prefix this: <http://rdf.disgenet.org/resource/nanopub/NP63986.RAPK_baNNMdJ-ICNVm8avuP6guanWxWB-UITAvgLV2epc> .
@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/> .
@prefix wi: <http://purl.org/ontology/wi/core#> .
@prefix prov: <http://www.w3.org/ns/prov#> .
@prefix pav: <http://purl.org/pav/> .
@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/resource/nanopub/> .
@prefix dgn-gda: <http://rdf.disgenet.org/resource/gda/> .
@prefix dgn-void: <http://rdf.disgenet.org/v3.0.0/void/> .

dgn-np:NP63986.RAPK_baNNMdJ-ICNVm8avuP6guanWxWB-UITAvgLV2epc130_head {
  this: np:hasAssertion dgn-np:NP63986.RAPK_baNNMdJ-ICNVm8avuP6guanWxWB-UITAvgLV2epc130_assertion;
    np:hasProvenance dgn-np:NP63986.RAPK_baNNMdJ-ICNVm8avuP6guanWxWB-UITAvgLV2epc130_provenance;
    np:hasPublicationInfo dgn-np:NP63986.RAPK_baNNMdJ-ICNVm8avuP6guanWxWB-UITAvgLV2epc130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP63986.RAPK_baNNMdJ-ICNVm8avuP6guanWxWB-UITAvgLV2epc130_assertion a np:Assertion .
  
  dgn-np:NP63986.RAPK_baNNMdJ-ICNVm8avuP6guanWxWB-UITAvgLV2epc130_provenance a np:Provenance .
  
  dgn-np:NP63986.RAPK_baNNMdJ-ICNVm8avuP6guanWxWB-UITAvgLV2epc130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP63986.RAPK_baNNMdJ-ICNVm8avuP6guanWxWB-UITAvgLV2epc130_assertion {
  miriam-gene:6532 a ncit:C16612 .
  
  lld:C0038644 a ncit:C7057 .
  
  dgn-gda:DGNa7721d72494ce37af0ef97dcb645ce54 sio:SIO_000628 miriam-gene:6532, lld:C0038644;
    a sio:SIO_001122 .
}

dgn-np:NP63986.RAPK_baNNMdJ-ICNVm8avuP6guanWxWB-UITAvgLV2epc130_provenance {
  dgn-np:NP63986.RAPK_baNNMdJ-ICNVm8avuP6guanWxWB-UITAvgLV2epc130_assertion dcterms:description
      "[This study, besides to delineate the cytoarchitecture and the localization in the brainstem of the human raphA(c) nuclei, aims to evaluate the correlation between neuropathological raphA(c) defects and serotonin transporter gene (5-HTT) promoter region polymorphisms in a cohort of 28 SIDS victims, 12 sudden intrauterine unexplained deaths (SIUD), and 17 controls.]. 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:19342987;
    prov:wasDerivedFrom dgn-void:gad-20150221;
    prov:wasGeneratedBy eco:ECO_0000203 .
  
  dgn-void:gad-20150221 pav:importedOn "2015-02-21"^^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:NP63986.RAPK_baNNMdJ-ICNVm8avuP6guanWxWB-UITAvgLV2epc130_publicationInfo {
  this: dcterms:created "2015-08-25T14:38:15+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:disgenetv3.0rdf;
    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 "v3.0.0.0" .
  
  dgn-void:disgenetv3.0rdf pav:version "v3.0.0" .
}