dgn-np:NP683010.RALpFPjC9EiIgkF0QNFIGVGb9JQqcp5VYoQdssHczKN5E130_provenance {
  dgn-np:NP683010.RALpFPjC9EiIgkF0QNFIGVGb9JQqcp5VYoQdssHczKN5E130_assertion dcterms:description "[This article will summarize how these new findings have expanded our understanding of whether diseases are homogeneous or heterogeneous entities (Bartter's syndrome versus Gitelman's syndrome), the medical basis of certain diseases of unclear etiology (enuresis), and the nature of risk factors for disease occurrence or progression (IgA nephropathy, chronic renal failure, and hemolytic uremic syndrome).]. 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:9203198 ;
    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 .
}