@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP87173.RAtaDDzyfr4sF1yTH-a08PbQc6MSmSxdxf98nm5BRtS20> .
@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:NP87173.RAtaDDzyfr4sF1yTH-a08PbQc6MSmSxdxf98nm5BRtS20130_head {
  this: np:hasAssertion dgn-np:NP87173.RAtaDDzyfr4sF1yTH-a08PbQc6MSmSxdxf98nm5BRtS20130_assertion ;
    np:hasProvenance dgn-np:NP87173.RAtaDDzyfr4sF1yTH-a08PbQc6MSmSxdxf98nm5BRtS20130_provenance ;
    np:hasPublicationInfo dgn-np:NP87173.RAtaDDzyfr4sF1yTH-a08PbQc6MSmSxdxf98nm5BRtS20130_publicationInfo ;
    a np:Nanopublication .
  dgn-np:NP87173.RAtaDDzyfr4sF1yTH-a08PbQc6MSmSxdxf98nm5BRtS20130_assertion a np:Assertion .
  dgn-np:NP87173.RAtaDDzyfr4sF1yTH-a08PbQc6MSmSxdxf98nm5BRtS20130_provenance a np:Provenance .
  dgn-np:NP87173.RAtaDDzyfr4sF1yTH-a08PbQc6MSmSxdxf98nm5BRtS20130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP87173.RAtaDDzyfr4sF1yTH-a08PbQc6MSmSxdxf98nm5BRtS20130_assertion {
  miriam-gene:8836 a ncit:C16612 .
  lld:C0553662 a ncit:C7057 .
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dgn-np:NP87173.RAtaDDzyfr4sF1yTH-a08PbQc6MSmSxdxf98nm5BRtS20130_provenance {
  dgn-np:NP87173.RAtaDDzyfr4sF1yTH-a08PbQc6MSmSxdxf98nm5BRtS20130_assertion dcterms:description "[The non-TT genotype at GGH T16C was associated with a high risk of liver dysfunction, presumably because the C allele of GGH C16T may reduce the activity of GGH. The time interval before MTX treatment and rheumatoid factor positivity were associated with the efficacy of MTX treatment. The pharmacogenetics of the MTX pathway genes affects the toxicity and efficacy of MTX in Japanese JIA patients.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ;
    wi:evidence dgn-void:source_evidence_literature ;
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    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 ;
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}
dgn-np:NP87173.RAtaDDzyfr4sF1yTH-a08PbQc6MSmSxdxf98nm5BRtS20130_publicationInfo {
  this: dcterms:created "2014-10-02T12:32:43+02:00"^^xsd:dateTime ;
    dcterms:rights <http://opendatacommons.org/licenses/odbl/1.0/> ;
    dcterms:rightsHolder dgn-void:IBIGroup ;
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}