@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP903398.RA-NlJNBb00kUiTX0ocRiAePPviu1be1pBi9BvxNLNibI> .
@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:NP903398.RA-NlJNBb00kUiTX0ocRiAePPviu1be1pBi9BvxNLNibI130_head {
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dgn-np:NP903398.RA-NlJNBb00kUiTX0ocRiAePPviu1be1pBi9BvxNLNibI130_assertion {
  miriam-gene:60498 a ncit:C16612 .
  
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dgn-np:NP903398.RA-NlJNBb00kUiTX0ocRiAePPviu1be1pBi9BvxNLNibI130_provenance {
  dgn-np:NP903398.RA-NlJNBb00kUiTX0ocRiAePPviu1be1pBi9BvxNLNibI130_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;
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dgn-np:NP903398.RA-NlJNBb00kUiTX0ocRiAePPviu1be1pBi9BvxNLNibI130_publicationInfo {
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