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- source_evidence_literature type ECO_0000212 NP1103898.RA2EDH9WwyFSkNE9DUp2MnLlmyLFdZ5FOlhmXWhCp-b3A130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP1103898.RA2EDH9WwyFSkNE9DUp2MnLlmyLFdZ5FOlhmXWhCp-b3A130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP1103898.RA2EDH9WwyFSkNE9DUp2MnLlmyLFdZ5FOlhmXWhCp-b3A130_provenance.
- NP1103898.RA2EDH9WwyFSkNE9DUp2MnLlmyLFdZ5FOlhmXWhCp-b3A130_assertion description "[Recently, we demonstrated that WNK4 is a substrate for KLHL3-Cullin3 (CUL3) E3 ubiquitin ligase complexes and that impaired WNK4 ubiquitination is a common mechanism for pseudohypoaldosteronism type II (PHAII) caused by WNK4, KLHL3, and CUL3 mutations.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1103898.RA2EDH9WwyFSkNE9DUp2MnLlmyLFdZ5FOlhmXWhCp-b3A130_provenance.
- NP1103898.RA2EDH9WwyFSkNE9DUp2MnLlmyLFdZ5FOlhmXWhCp-b3A130_assertion evidence source_evidence_literature NP1103898.RA2EDH9WwyFSkNE9DUp2MnLlmyLFdZ5FOlhmXWhCp-b3A130_provenance.
- NP1103898.RA2EDH9WwyFSkNE9DUp2MnLlmyLFdZ5FOlhmXWhCp-b3A130_assertion SIO_000772 23962426 NP1103898.RA2EDH9WwyFSkNE9DUp2MnLlmyLFdZ5FOlhmXWhCp-b3A130_provenance.
- NP1103898.RA2EDH9WwyFSkNE9DUp2MnLlmyLFdZ5FOlhmXWhCp-b3A130_assertion wasDerivedFrom befree-2016 NP1103898.RA2EDH9WwyFSkNE9DUp2MnLlmyLFdZ5FOlhmXWhCp-b3A130_provenance.
- NP1103898.RA2EDH9WwyFSkNE9DUp2MnLlmyLFdZ5FOlhmXWhCp-b3A130_assertion wasGeneratedBy ECO_0000203 NP1103898.RA2EDH9WwyFSkNE9DUp2MnLlmyLFdZ5FOlhmXWhCp-b3A130_provenance.
- befree-2016 importedOn "2016-02-19" NP1103898.RA2EDH9WwyFSkNE9DUp2MnLlmyLFdZ5FOlhmXWhCp-b3A130_provenance.