@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP589239.RACMbjgIGyCl26owvTBcO3j5KO_IUvSRuJ4unM1zv89Kw> .
@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:NP589239.RACMbjgIGyCl26owvTBcO3j5KO_IUvSRuJ4unM1zv89Kw130_head {
  this: np:hasAssertion dgn-np:NP589239.RACMbjgIGyCl26owvTBcO3j5KO_IUvSRuJ4unM1zv89Kw130_assertion ;
    np:hasProvenance dgn-np:NP589239.RACMbjgIGyCl26owvTBcO3j5KO_IUvSRuJ4unM1zv89Kw130_provenance ;
    np:hasPublicationInfo dgn-np:NP589239.RACMbjgIGyCl26owvTBcO3j5KO_IUvSRuJ4unM1zv89Kw130_publicationInfo ;
    a np:Nanopublication .
  dgn-np:NP589239.RACMbjgIGyCl26owvTBcO3j5KO_IUvSRuJ4unM1zv89Kw130_assertion a np:Assertion .
  dgn-np:NP589239.RACMbjgIGyCl26owvTBcO3j5KO_IUvSRuJ4unM1zv89Kw130_provenance a np:Provenance .
  dgn-np:NP589239.RACMbjgIGyCl26owvTBcO3j5KO_IUvSRuJ4unM1zv89Kw130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP589239.RACMbjgIGyCl26owvTBcO3j5KO_IUvSRuJ4unM1zv89Kw130_assertion {
  miriam-gene:5743 a ncit:C16612 .
  lld:C0184567 a ncit:C7057 .
  dgn-gda:DGN5648083287d6b13970e6242ec0475011 sio:SIO_000628 miriam-gene:5743 , lld:C0184567 ;
    a sio:SIO_001121 .
}
dgn-np:NP589239.RACMbjgIGyCl26owvTBcO3j5KO_IUvSRuJ4unM1zv89Kw130_provenance {
  dgn-np:NP589239.RACMbjgIGyCl26owvTBcO3j5KO_IUvSRuJ4unM1zv89Kw130_assertion dcterms:description "[These results suggest that wide variability in gene expression and functional polymorphisms in PTGS2 may explain part of the interindividual variations in acute pain and the analgesic efficacy of nonsteroidal anti-inflammatory drugs and selective COX-2 inhibitors; this may be useful to define individual responders on the basis of genetic variations to predict patient risk and benefit to drugs.]. 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:16678543 ;
    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:NP589239.RACMbjgIGyCl26owvTBcO3j5KO_IUvSRuJ4unM1zv89Kw130_publicationInfo {
  this: dcterms:created "2014-10-02T12:37:54+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" .
}