@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP223971.RAv_sa2Djg70QuPgoTJ2DnGADoBnFzZ9PqJrScDJ-mdok> .
@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:NP223971.RAv_sa2Djg70QuPgoTJ2DnGADoBnFzZ9PqJrScDJ-mdok130_head {
  this: np:hasAssertion dgn-np:NP223971.RAv_sa2Djg70QuPgoTJ2DnGADoBnFzZ9PqJrScDJ-mdok130_assertion;
    np:hasProvenance dgn-np:NP223971.RAv_sa2Djg70QuPgoTJ2DnGADoBnFzZ9PqJrScDJ-mdok130_provenance;
    np:hasPublicationInfo dgn-np:NP223971.RAv_sa2Djg70QuPgoTJ2DnGADoBnFzZ9PqJrScDJ-mdok130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP223971.RAv_sa2Djg70QuPgoTJ2DnGADoBnFzZ9PqJrScDJ-mdok130_assertion a np:Assertion .
  
  dgn-np:NP223971.RAv_sa2Djg70QuPgoTJ2DnGADoBnFzZ9PqJrScDJ-mdok130_provenance a np:Provenance .
  
  dgn-np:NP223971.RAv_sa2Djg70QuPgoTJ2DnGADoBnFzZ9PqJrScDJ-mdok130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP223971.RAv_sa2Djg70QuPgoTJ2DnGADoBnFzZ9PqJrScDJ-mdok130_assertion {
  miriam-gene:10249 a ncit:C16612 .
  
  lld:C1260386 a ncit:C7057 .
  
  dgn-gda:DGNd5035863f6b847c713394c9fd0947f90 sio:SIO_000628 miriam-gene:10249, lld:C1260386;
    a sio:SIO_001121 .
}

dgn-np:NP223971.RAv_sa2Djg70QuPgoTJ2DnGADoBnFzZ9PqJrScDJ-mdok130_provenance {
  dgn-np:NP223971.RAv_sa2Djg70QuPgoTJ2DnGADoBnFzZ9PqJrScDJ-mdok130_assertion dcterms:description
      "[In higher GSH deficiency (> 40 %) with increased ROS generation, Cp expression was decreased due to promotion of Cp mRNA decay mediated by 3'untranslated region (3'UTR) as found by transfecting chimera of chloramphenicol acetyl transferase (CAT) gene with Cp 3'UTR.]. 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:20211720;
    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:NP223971.RAv_sa2Djg70QuPgoTJ2DnGADoBnFzZ9PqJrScDJ-mdok130_publicationInfo {
  this: dcterms:created "2014-10-02T12:34:04+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" .
}