@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP59941.RARw1YAgC9JMKkXVuY5Sc1ddSfDnExB6K2MvdF0prsDxs> .
@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:NP59941.RARw1YAgC9JMKkXVuY5Sc1ddSfDnExB6K2MvdF0prsDxs130_head {
   this: np:hasAssertion dgn-np:NP59941.RARw1YAgC9JMKkXVuY5Sc1ddSfDnExB6K2MvdF0prsDxs130_assertion ;
    np:hasProvenance dgn-np:NP59941.RARw1YAgC9JMKkXVuY5Sc1ddSfDnExB6K2MvdF0prsDxs130_provenance ;
    np:hasPublicationInfo dgn-np:NP59941.RARw1YAgC9JMKkXVuY5Sc1ddSfDnExB6K2MvdF0prsDxs130_publicationInfo ;
    a np:Nanopublication .
  dgn-np:NP59941.RARw1YAgC9JMKkXVuY5Sc1ddSfDnExB6K2MvdF0prsDxs130_assertion a np:Assertion .
  dgn-np:NP59941.RARw1YAgC9JMKkXVuY5Sc1ddSfDnExB6K2MvdF0prsDxs130_provenance a np:Provenance .
  dgn-np:NP59941.RARw1YAgC9JMKkXVuY5Sc1ddSfDnExB6K2MvdF0prsDxs130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP59941.RARw1YAgC9JMKkXVuY5Sc1ddSfDnExB6K2MvdF0prsDxs130_assertion {
   miriam-gene:1312 a ncit:C16612 .
  lld:C0030319 a ncit:C7057 .
  dgn-gda:DGN7d29491d45999bbcaa1bc8c90def0c90 sio:SIO_000628 miriam-gene:1312 , lld:C0030319 ;
    a sio:SIO_001122 .
}
dgn-np:NP59941.RARw1YAgC9JMKkXVuY5Sc1ddSfDnExB6K2MvdF0prsDxs130_provenance {
   dgn-np:NP59941.RARw1YAgC9JMKkXVuY5Sc1ddSfDnExB6K2MvdF0prsDxs130_assertion dcterms:description "[To further evaluate the influence of the Val158Met COMT polymorphism in panic disorder we genotyped this marker in the coding region of the COMT gene and two additional variants (rs737865 and rs165599) in the 5' and the 3' region, respectively, in two independent Canadian samples: 121 nuclear families, and 89 cases with matched 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:16525418 ;
    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:NP59941.RARw1YAgC9JMKkXVuY5Sc1ddSfDnExB6K2MvdF0prsDxs130_publicationInfo {
   this: dcterms:created "2014-10-02T12:32:28+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" .
}