@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP318527.RAzEEh0-woX7Llib__WKHBbOLD6INbBFFRApZDE9rkvmU> .
@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:NP318527.RAzEEh0-woX7Llib__WKHBbOLD6INbBFFRApZDE9rkvmU130_head {
  this: np:hasAssertion dgn-np:NP318527.RAzEEh0-woX7Llib__WKHBbOLD6INbBFFRApZDE9rkvmU130_assertion;
    np:hasProvenance dgn-np:NP318527.RAzEEh0-woX7Llib__WKHBbOLD6INbBFFRApZDE9rkvmU130_provenance;
    np:hasPublicationInfo dgn-np:NP318527.RAzEEh0-woX7Llib__WKHBbOLD6INbBFFRApZDE9rkvmU130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP318527.RAzEEh0-woX7Llib__WKHBbOLD6INbBFFRApZDE9rkvmU130_assertion a np:Assertion .
  
  dgn-np:NP318527.RAzEEh0-woX7Llib__WKHBbOLD6INbBFFRApZDE9rkvmU130_provenance a np:Provenance .
  
  dgn-np:NP318527.RAzEEh0-woX7Llib__WKHBbOLD6INbBFFRApZDE9rkvmU130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP318527.RAzEEh0-woX7Llib__WKHBbOLD6INbBFFRApZDE9rkvmU130_assertion {
  miriam-gene:9177 a ncit:C16612 .
  
  lld:C0036341 a ncit:C7057 .
  
  dgn-gda:DGNe556bbdab5ec1b31cc679b60231e302e sio:SIO_000628 miriam-gene:9177, lld:C0036341;
    a sio:SIO_001121 .
}

dgn-np:NP318527.RAzEEh0-woX7Llib__WKHBbOLD6INbBFFRApZDE9rkvmU130_provenance {
  dgn-np:NP318527.RAzEEh0-woX7Llib__WKHBbOLD6INbBFFRApZDE9rkvmU130_assertion dcterms:description
      "[We evaluated whether genetic variants in the serotonin receptors HTR3A (rs897692, rs1150226, rs1176724, rs2276302, rs3737457, rs897687 and rs1176713) and HTR3B (rs3758987, rs10502180, rs11606194, rs17116121, rs1176744, rs17116138, rs2276307, rs3782025 and rs1176761) were susceptibility components for suicidal behavior in 154 Caucasians schizophrenia subjects (20.1% of suicide attempters).]. 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:21184810;
    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:NP318527.RAzEEh0-woX7Llib__WKHBbOLD6INbBFFRApZDE9rkvmU130_publicationInfo {
  this: dcterms:created "2014-10-02T12:35:04+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" .
}