Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP382234.RAu4-10bF2IFtN4qzaxge8IMhA7wYoImu4TVvi_VkiJGE130_assertion> ?p ?o ?g. }
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- NP382234.RAu4-10bF2IFtN4qzaxge8IMhA7wYoImu4TVvi_VkiJGE130_assertion type Assertion NP382234.RAu4-10bF2IFtN4qzaxge8IMhA7wYoImu4TVvi_VkiJGE130_head.
- NP382234.RAu4-10bF2IFtN4qzaxge8IMhA7wYoImu4TVvi_VkiJGE130_assertion wasGeneratedBy ECO_0000203 NP382234.RAu4-10bF2IFtN4qzaxge8IMhA7wYoImu4TVvi_VkiJGE130_provenance.
- NP382234.RAu4-10bF2IFtN4qzaxge8IMhA7wYoImu4TVvi_VkiJGE130_assertion wasDerivedFrom befree-20140225 NP382234.RAu4-10bF2IFtN4qzaxge8IMhA7wYoImu4TVvi_VkiJGE130_provenance.
- NP382234.RAu4-10bF2IFtN4qzaxge8IMhA7wYoImu4TVvi_VkiJGE130_assertion SIO_000772 9727001 NP382234.RAu4-10bF2IFtN4qzaxge8IMhA7wYoImu4TVvi_VkiJGE130_provenance.
- NP382234.RAu4-10bF2IFtN4qzaxge8IMhA7wYoImu4TVvi_VkiJGE130_assertion evidence source_evidence_literature NP382234.RAu4-10bF2IFtN4qzaxge8IMhA7wYoImu4TVvi_VkiJGE130_provenance.
- NP382234.RAu4-10bF2IFtN4qzaxge8IMhA7wYoImu4TVvi_VkiJGE130_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." NP382234.RAu4-10bF2IFtN4qzaxge8IMhA7wYoImu4TVvi_VkiJGE130_provenance.