Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP1403338.RATrHKKEjQsDC3L-MjcvT3r5oykTg7nO07709kFYBFzno130_assertion> ?p ?o ?g. }
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- NP1403338.RATrHKKEjQsDC3L-MjcvT3r5oykTg7nO07709kFYBFzno130_assertion type Assertion NP1403338.RATrHKKEjQsDC3L-MjcvT3r5oykTg7nO07709kFYBFzno130_head.
- NP1403338.RATrHKKEjQsDC3L-MjcvT3r5oykTg7nO07709kFYBFzno130_assertion wasGeneratedBy ECO_0000203 NP1403338.RATrHKKEjQsDC3L-MjcvT3r5oykTg7nO07709kFYBFzno130_provenance.
- NP1403338.RATrHKKEjQsDC3L-MjcvT3r5oykTg7nO07709kFYBFzno130_assertion wasDerivedFrom befree-2016 NP1403338.RATrHKKEjQsDC3L-MjcvT3r5oykTg7nO07709kFYBFzno130_provenance.
- NP1403338.RATrHKKEjQsDC3L-MjcvT3r5oykTg7nO07709kFYBFzno130_assertion SIO_000772 9727001 NP1403338.RATrHKKEjQsDC3L-MjcvT3r5oykTg7nO07709kFYBFzno130_provenance.
- NP1403338.RATrHKKEjQsDC3L-MjcvT3r5oykTg7nO07709kFYBFzno130_assertion evidence source_evidence_literature NP1403338.RATrHKKEjQsDC3L-MjcvT3r5oykTg7nO07709kFYBFzno130_provenance.
- NP1403338.RATrHKKEjQsDC3L-MjcvT3r5oykTg7nO07709kFYBFzno130_assertion description "[Loss of function mutations in kidney Kir1.1 (renal outer medullary potassium channel, KCNJ1) inwardly rectifying potassium channels can be found in patients suffering from hyperprostaglandin E syndrome (HPS), the antenatal form of Bartter syndrome.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1403338.RATrHKKEjQsDC3L-MjcvT3r5oykTg7nO07709kFYBFzno130_provenance.