@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP404083.RAYxzPzLiOIyiiJgTca8-E9f1j5hJ1Jh0kTHZXjQt05SY> .
@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:NP404083.RAYxzPzLiOIyiiJgTca8-E9f1j5hJ1Jh0kTHZXjQt05SY130_head {
  this: np:hasAssertion dgn-np:NP404083.RAYxzPzLiOIyiiJgTca8-E9f1j5hJ1Jh0kTHZXjQt05SY130_assertion;
    np:hasProvenance dgn-np:NP404083.RAYxzPzLiOIyiiJgTca8-E9f1j5hJ1Jh0kTHZXjQt05SY130_provenance;
    np:hasPublicationInfo dgn-np:NP404083.RAYxzPzLiOIyiiJgTca8-E9f1j5hJ1Jh0kTHZXjQt05SY130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP404083.RAYxzPzLiOIyiiJgTca8-E9f1j5hJ1Jh0kTHZXjQt05SY130_assertion a np:Assertion .
  
  dgn-np:NP404083.RAYxzPzLiOIyiiJgTca8-E9f1j5hJ1Jh0kTHZXjQt05SY130_provenance a np:Provenance .
  
  dgn-np:NP404083.RAYxzPzLiOIyiiJgTca8-E9f1j5hJ1Jh0kTHZXjQt05SY130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP404083.RAYxzPzLiOIyiiJgTca8-E9f1j5hJ1Jh0kTHZXjQt05SY130_assertion {
  miriam-gene:2937 a ncit:C16612 .
  
  lld:C1260386 a ncit:C7057 .
  
  dgn-gda:DGN40dc886ec31f5fe2855e484d62a21923 sio:SIO_000628 miriam-gene:2937, lld:C1260386;
    a sio:SIO_001121 .
}

dgn-np:NP404083.RAYxzPzLiOIyiiJgTca8-E9f1j5hJ1Jh0kTHZXjQt05SY130_provenance {
  dgn-np:NP404083.RAYxzPzLiOIyiiJgTca8-E9f1j5hJ1Jh0kTHZXjQt05SY130_assertion dcterms:description
      "[We conclude that the primary defect is one of GSH-S. Glutathione stabilizes GST in vitro, and it is assumed that the deficiency of GST in the erythrocytes of the patients is due to the instability of this enzyme in the absence of adequate intracellular GSH levels.]. 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:3944259;
    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:NP404083.RAYxzPzLiOIyiiJgTca8-E9f1j5hJ1Jh0kTHZXjQt05SY130_publicationInfo {
  this: dcterms:created "2014-10-02T12:36:00+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" .
}