Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP723248.RADMjsSVJ8A7svdzYkrU9crALAo2L9VNmsOUxDcqdHWb8130_assertion> ?p ?o ?g. }
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- NP723248.RADMjsSVJ8A7svdzYkrU9crALAo2L9VNmsOUxDcqdHWb8130_assertion type Assertion NP723248.RADMjsSVJ8A7svdzYkrU9crALAo2L9VNmsOUxDcqdHWb8130_head.
- NP723248.RADMjsSVJ8A7svdzYkrU9crALAo2L9VNmsOUxDcqdHWb8130_assertion description "[This study revealed the following characteristics of these disorders: 1) subjects with CLCNKB mutations showed one or more biochemical features of Gitelman syndrome (including hypomagnesemia, hypocalciuria, and fractional chloride excretion insensitivity to thiazide administration); and 2) subjects with KCNJ1 mutations appeared to show normal fractional chloride excretion sensitivity to furosemide and thiazide administration.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP723248.RADMjsSVJ8A7svdzYkrU9crALAo2L9VNmsOUxDcqdHWb8130_provenance.
- NP723248.RADMjsSVJ8A7svdzYkrU9crALAo2L9VNmsOUxDcqdHWb8130_assertion evidence source_evidence_literature NP723248.RADMjsSVJ8A7svdzYkrU9crALAo2L9VNmsOUxDcqdHWb8130_provenance.
- NP723248.RADMjsSVJ8A7svdzYkrU9crALAo2L9VNmsOUxDcqdHWb8130_assertion SIO_000772 20810575 NP723248.RADMjsSVJ8A7svdzYkrU9crALAo2L9VNmsOUxDcqdHWb8130_provenance.
- NP723248.RADMjsSVJ8A7svdzYkrU9crALAo2L9VNmsOUxDcqdHWb8130_assertion wasDerivedFrom befree-20140225 NP723248.RADMjsSVJ8A7svdzYkrU9crALAo2L9VNmsOUxDcqdHWb8130_provenance.
- NP723248.RADMjsSVJ8A7svdzYkrU9crALAo2L9VNmsOUxDcqdHWb8130_assertion wasGeneratedBy ECO_0000203 NP723248.RADMjsSVJ8A7svdzYkrU9crALAo2L9VNmsOUxDcqdHWb8130_provenance.