Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP492602.RAffT98RANFicZ5h4zv0axHNzcOISlAw0LvfExZImP1P4130_assertion> ?p ?o ?g. }
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- NP492602.RAffT98RANFicZ5h4zv0axHNzcOISlAw0LvfExZImP1P4130_assertion type Assertion NP492602.RAffT98RANFicZ5h4zv0axHNzcOISlAw0LvfExZImP1P4130_head.
- NP492602.RAffT98RANFicZ5h4zv0axHNzcOISlAw0LvfExZImP1P4130_assertion description "[Two WNK isoforms, WNK1 and WNK4, have been identified as the disease genes for a rare monogenic hypertension syndrome (Gordon's syndrome or pseudohypoaldosteronism type 2 [PHA2]) implicating them in salt homeostasis by the kidney.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP492602.RAffT98RANFicZ5h4zv0axHNzcOISlAw0LvfExZImP1P4130_provenance.
- NP492602.RAffT98RANFicZ5h4zv0axHNzcOISlAw0LvfExZImP1P4130_assertion evidence source_evidence_literature NP492602.RAffT98RANFicZ5h4zv0axHNzcOISlAw0LvfExZImP1P4130_provenance.
- NP492602.RAffT98RANFicZ5h4zv0axHNzcOISlAw0LvfExZImP1P4130_assertion SIO_000772 15866321 NP492602.RAffT98RANFicZ5h4zv0axHNzcOISlAw0LvfExZImP1P4130_provenance.
- NP492602.RAffT98RANFicZ5h4zv0axHNzcOISlAw0LvfExZImP1P4130_assertion wasDerivedFrom befree-2016 NP492602.RAffT98RANFicZ5h4zv0axHNzcOISlAw0LvfExZImP1P4130_provenance.
- NP492602.RAffT98RANFicZ5h4zv0axHNzcOISlAw0LvfExZImP1P4130_assertion wasGeneratedBy ECO_0000203 NP492602.RAffT98RANFicZ5h4zv0axHNzcOISlAw0LvfExZImP1P4130_provenance.