@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP286886.RAhsZ2N4BA-toV9pXA3lFP2BvCtefapOpGBEkdJxWLPH8> .
@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:NP286886.RAhsZ2N4BA-toV9pXA3lFP2BvCtefapOpGBEkdJxWLPH8130_head {
  this: np:hasAssertion dgn-np:NP286886.RAhsZ2N4BA-toV9pXA3lFP2BvCtefapOpGBEkdJxWLPH8130_assertion ;
    np:hasProvenance dgn-np:NP286886.RAhsZ2N4BA-toV9pXA3lFP2BvCtefapOpGBEkdJxWLPH8130_provenance ;
    np:hasPublicationInfo dgn-np:NP286886.RAhsZ2N4BA-toV9pXA3lFP2BvCtefapOpGBEkdJxWLPH8130_publicationInfo ;
    a np:Nanopublication .
  dgn-np:NP286886.RAhsZ2N4BA-toV9pXA3lFP2BvCtefapOpGBEkdJxWLPH8130_assertion a np:Assertion .
  dgn-np:NP286886.RAhsZ2N4BA-toV9pXA3lFP2BvCtefapOpGBEkdJxWLPH8130_provenance a np:Provenance .
  dgn-np:NP286886.RAhsZ2N4BA-toV9pXA3lFP2BvCtefapOpGBEkdJxWLPH8130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP286886.RAhsZ2N4BA-toV9pXA3lFP2BvCtefapOpGBEkdJxWLPH8130_assertion {
  miriam-gene:1312 a ncit:C16612 .
  lld:C0030319 a ncit:C7057 .
  dgn-gda:DGN7a3108be194299edfc7df5f8e9c7648f sio:SIO_000628 miriam-gene:1312 , lld:C0030319 ;
    a sio:SIO_001121 .
}
dgn-np:NP286886.RAhsZ2N4BA-toV9pXA3lFP2BvCtefapOpGBEkdJxWLPH8130_provenance {
  dgn-np:NP286886.RAhsZ2N4BA-toV9pXA3lFP2BvCtefapOpGBEkdJxWLPH8130_assertion dcterms:description "[In the present study, a meta-analysis of six available case-control studies (557 patients with panic disorder and 763 healthy controls in total) on the role of the COMT val158met polymorphism in panic disorder was conducted in an attempt to reconcile previous conflicting results and to facilitate evaluation of the role of COMT gene variation in panic disorder.]. 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:17357147 ;
    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:NP286886.RAhsZ2N4BA-toV9pXA3lFP2BvCtefapOpGBEkdJxWLPH8130_publicationInfo {
  this: dcterms:created "2014-10-02T12:34:43+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> ;
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    pav:version "v2.1.0.0" .
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}