@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP643142.RAAbOfpdCExDnbySpt3rRXe7Bi56i2dhTFNnUVgHWlhs4> .
@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:NP643142.RAAbOfpdCExDnbySpt3rRXe7Bi56i2dhTFNnUVgHWlhs4130_head {
  this: np:hasAssertion dgn-np:NP643142.RAAbOfpdCExDnbySpt3rRXe7Bi56i2dhTFNnUVgHWlhs4130_assertion;
    np:hasProvenance dgn-np:NP643142.RAAbOfpdCExDnbySpt3rRXe7Bi56i2dhTFNnUVgHWlhs4130_provenance;
    np:hasPublicationInfo dgn-np:NP643142.RAAbOfpdCExDnbySpt3rRXe7Bi56i2dhTFNnUVgHWlhs4130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP643142.RAAbOfpdCExDnbySpt3rRXe7Bi56i2dhTFNnUVgHWlhs4130_assertion a np:Assertion .
  
  dgn-np:NP643142.RAAbOfpdCExDnbySpt3rRXe7Bi56i2dhTFNnUVgHWlhs4130_provenance a np:Provenance .
  
  dgn-np:NP643142.RAAbOfpdCExDnbySpt3rRXe7Bi56i2dhTFNnUVgHWlhs4130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP643142.RAAbOfpdCExDnbySpt3rRXe7Bi56i2dhTFNnUVgHWlhs4130_assertion {
  miriam-gene:885 a ncit:C16612 .
  
  lld:C0233777 a ncit:C7057 .
  
  dgn-gda:DGN8fee1493deaf1724e55875ad00ffedb7 sio:SIO_000628 miriam-gene:885, lld:C0233777;
    a sio:SIO_001121 .
}

dgn-np:NP643142.RAAbOfpdCExDnbySpt3rRXe7Bi56i2dhTFNnUVgHWlhs4130_provenance {
  dgn-np:NP643142.RAAbOfpdCExDnbySpt3rRXe7Bi56i2dhTFNnUVgHWlhs4130_assertion dcterms:description
      "[In this study, we examined the genetic variant -45 C to T substitution of the CCK gene promoter region among 195 healthy Japanese and 174 patients with alcohol withdrawal syndrome (52 delirium tremens, 39 hallucinosis, 20 seizures, and 92 lack of these symptoms) by using polymerase chain reaction-based single-strand conformational polymorphism analysis.]. 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:10235270;
    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:NP643142.RAAbOfpdCExDnbySpt3rRXe7Bi56i2dhTFNnUVgHWlhs4130_publicationInfo {
  this: dcterms:created "2014-10-02T12:38:27+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" .
}