Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP877439.RAE37TLO5MVILWP6Jh4dD0J2Ke75shr4B3BuptmrlFeaM130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP877439.RAE37TLO5MVILWP6Jh4dD0J2Ke75shr4B3BuptmrlFeaM130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP877439.RAE37TLO5MVILWP6Jh4dD0J2Ke75shr4B3BuptmrlFeaM130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP877439.RAE37TLO5MVILWP6Jh4dD0J2Ke75shr4B3BuptmrlFeaM130_provenance.
- NP877439.RAE37TLO5MVILWP6Jh4dD0J2Ke75shr4B3BuptmrlFeaM130_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." NP877439.RAE37TLO5MVILWP6Jh4dD0J2Ke75shr4B3BuptmrlFeaM130_provenance.
- NP877439.RAE37TLO5MVILWP6Jh4dD0J2Ke75shr4B3BuptmrlFeaM130_assertion evidence source_evidence_literature NP877439.RAE37TLO5MVILWP6Jh4dD0J2Ke75shr4B3BuptmrlFeaM130_provenance.
- NP877439.RAE37TLO5MVILWP6Jh4dD0J2Ke75shr4B3BuptmrlFeaM130_assertion SIO_000772 23962426 NP877439.RAE37TLO5MVILWP6Jh4dD0J2Ke75shr4B3BuptmrlFeaM130_provenance.
- NP877439.RAE37TLO5MVILWP6Jh4dD0J2Ke75shr4B3BuptmrlFeaM130_assertion wasDerivedFrom befree-20140225 NP877439.RAE37TLO5MVILWP6Jh4dD0J2Ke75shr4B3BuptmrlFeaM130_provenance.
- NP877439.RAE37TLO5MVILWP6Jh4dD0J2Ke75shr4B3BuptmrlFeaM130_assertion wasGeneratedBy ECO_0000203 NP877439.RAE37TLO5MVILWP6Jh4dD0J2Ke75shr4B3BuptmrlFeaM130_provenance.
- befree-20140225 importedOn "2014-02-25" NP877439.RAE37TLO5MVILWP6Jh4dD0J2Ke75shr4B3BuptmrlFeaM130_provenance.