@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP47492.RAYe3ArHnaTSI1_OEThfymfmS0suviVrlzNeSTfvvZ7qg> .
@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:NP47492.RAYe3ArHnaTSI1_OEThfymfmS0suviVrlzNeSTfvvZ7qg130_head {
  this: np:hasAssertion dgn-np:NP47492.RAYe3ArHnaTSI1_OEThfymfmS0suviVrlzNeSTfvvZ7qg130_assertion;
    np:hasProvenance dgn-np:NP47492.RAYe3ArHnaTSI1_OEThfymfmS0suviVrlzNeSTfvvZ7qg130_provenance;
    np:hasPublicationInfo dgn-np:NP47492.RAYe3ArHnaTSI1_OEThfymfmS0suviVrlzNeSTfvvZ7qg130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP47492.RAYe3ArHnaTSI1_OEThfymfmS0suviVrlzNeSTfvvZ7qg130_assertion a np:Assertion .
  
  dgn-np:NP47492.RAYe3ArHnaTSI1_OEThfymfmS0suviVrlzNeSTfvvZ7qg130_provenance a np:Provenance .
  
  dgn-np:NP47492.RAYe3ArHnaTSI1_OEThfymfmS0suviVrlzNeSTfvvZ7qg130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP47492.RAYe3ArHnaTSI1_OEThfymfmS0suviVrlzNeSTfvvZ7qg130_assertion {
  miriam-gene:885 a ncit:C16612 .
  
  lld:C0030319 a ncit:C7057 .
  
  dgn-gda:DGN67053833dea4d5da03c197277227c004 sio:SIO_000628 miriam-gene:885, lld:C0030319;
    a sio:SIO_001122 .
}

dgn-np:NP47492.RAYe3ArHnaTSI1_OEThfymfmS0suviVrlzNeSTfvvZ7qg130_provenance {
  dgn-np:NP47492.RAYe3ArHnaTSI1_OEThfymfmS0suviVrlzNeSTfvvZ7qg130_assertion dcterms:description
      "[An association between the CCK polymorphism and panic disorder cannot be considered established due to the inconsistencies in the results noted above, but if the provisional association can be replicated, the findings are consistent with CCK(-36C-->T) being a disease-susceptibility allele that alone is neither necessary nor sufficient to cause panic disorder but that increases vulnerability by acting epistatically.]. 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:9603610;
    prov:wasDerivedFrom dgn-void:gad-20130706;
    prov:wasGeneratedBy eco:ECO_0000203 .
  
  dgn-void:gad-20130706 pav:importedOn "2013-07-06"^^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:NP47492.RAYe3ArHnaTSI1_OEThfymfmS0suviVrlzNeSTfvvZ7qg130_publicationInfo {
  this: dcterms:created "2014-10-02T12:32:21+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" .
}