Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP315491.RAkUNVU9gb7FnOgLmzmscuU6zqxyUUohnGjv0Y2EAbLwQ130_assertion> ?p ?o ?g. }
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- NP315491.RAkUNVU9gb7FnOgLmzmscuU6zqxyUUohnGjv0Y2EAbLwQ130_assertion type Assertion NP315491.RAkUNVU9gb7FnOgLmzmscuU6zqxyUUohnGjv0Y2EAbLwQ130_head.
- NP315491.RAkUNVU9gb7FnOgLmzmscuU6zqxyUUohnGjv0Y2EAbLwQ130_assertion wasGeneratedBy ECO_0000203 NP315491.RAkUNVU9gb7FnOgLmzmscuU6zqxyUUohnGjv0Y2EAbLwQ130_provenance.
- NP315491.RAkUNVU9gb7FnOgLmzmscuU6zqxyUUohnGjv0Y2EAbLwQ130_assertion wasDerivedFrom befree-20150227 NP315491.RAkUNVU9gb7FnOgLmzmscuU6zqxyUUohnGjv0Y2EAbLwQ130_provenance.
- NP315491.RAkUNVU9gb7FnOgLmzmscuU6zqxyUUohnGjv0Y2EAbLwQ130_assertion SIO_000772 10831588 NP315491.RAkUNVU9gb7FnOgLmzmscuU6zqxyUUohnGjv0Y2EAbLwQ130_provenance.
- NP315491.RAkUNVU9gb7FnOgLmzmscuU6zqxyUUohnGjv0Y2EAbLwQ130_assertion evidence source_evidence_literature NP315491.RAkUNVU9gb7FnOgLmzmscuU6zqxyUUohnGjv0Y2EAbLwQ130_provenance.
- NP315491.RAkUNVU9gb7FnOgLmzmscuU6zqxyUUohnGjv0Y2EAbLwQ130_assertion description "[Genetic evidence suggests their involvement in transepithelial transport of chloride in distal nephron segments; ClC-K1 gene deletion leads to nephrogenic diabetes insipidus in mice, and mutations of the hClC-Kb gene cause Bartter's syndrome type III in humans.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP315491.RAkUNVU9gb7FnOgLmzmscuU6zqxyUUohnGjv0Y2EAbLwQ130_provenance.