Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP368338.RATYd4xTfLqRlays3qsty6SaTSSjead4ebrXI4mZoTvmY130_assertion> ?p ?o ?g. }
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- NP368338.RATYd4xTfLqRlays3qsty6SaTSSjead4ebrXI4mZoTvmY130_assertion type Assertion NP368338.RATYd4xTfLqRlays3qsty6SaTSSjead4ebrXI4mZoTvmY130_head.
- NP368338.RATYd4xTfLqRlays3qsty6SaTSSjead4ebrXI4mZoTvmY130_assertion description "[Genetic studies in humans have shown that large intronic deletions in WNK1 lead to its overexpression and are responsible for pseudohypoaldosteronism type II, an autosomal dominant disorder characterized by hypertension, increased renal salt reabsorption, and impaired K+ and H+ excretion.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP368338.RATYd4xTfLqRlays3qsty6SaTSSjead4ebrXI4mZoTvmY130_provenance.
- NP368338.RATYd4xTfLqRlays3qsty6SaTSSjead4ebrXI4mZoTvmY130_assertion evidence source_evidence_literature NP368338.RATYd4xTfLqRlays3qsty6SaTSSjead4ebrXI4mZoTvmY130_provenance.
- NP368338.RATYd4xTfLqRlays3qsty6SaTSSjead4ebrXI4mZoTvmY130_assertion SIO_000772 14610273 NP368338.RATYd4xTfLqRlays3qsty6SaTSSjead4ebrXI4mZoTvmY130_provenance.
- NP368338.RATYd4xTfLqRlays3qsty6SaTSSjead4ebrXI4mZoTvmY130_assertion wasDerivedFrom befree-20140225 NP368338.RATYd4xTfLqRlays3qsty6SaTSSjead4ebrXI4mZoTvmY130_provenance.
- NP368338.RATYd4xTfLqRlays3qsty6SaTSSjead4ebrXI4mZoTvmY130_assertion wasGeneratedBy ECO_0000203 NP368338.RATYd4xTfLqRlays3qsty6SaTSSjead4ebrXI4mZoTvmY130_provenance.