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- source_evidence_literature type ECO_0000212 NP976963.RAyP3rmhDqMGYiWanXHFAP3wfGrM0Xx_4N74zxbfO79Yk130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP976963.RAyP3rmhDqMGYiWanXHFAP3wfGrM0Xx_4N74zxbfO79Yk130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP976963.RAyP3rmhDqMGYiWanXHFAP3wfGrM0Xx_4N74zxbfO79Yk130_provenance.
- NP976963.RAyP3rmhDqMGYiWanXHFAP3wfGrM0Xx_4N74zxbfO79Yk130_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." NP976963.RAyP3rmhDqMGYiWanXHFAP3wfGrM0Xx_4N74zxbfO79Yk130_provenance.
- NP976963.RAyP3rmhDqMGYiWanXHFAP3wfGrM0Xx_4N74zxbfO79Yk130_assertion evidence source_evidence_literature NP976963.RAyP3rmhDqMGYiWanXHFAP3wfGrM0Xx_4N74zxbfO79Yk130_provenance.
- NP976963.RAyP3rmhDqMGYiWanXHFAP3wfGrM0Xx_4N74zxbfO79Yk130_assertion SIO_000772 23962426 NP976963.RAyP3rmhDqMGYiWanXHFAP3wfGrM0Xx_4N74zxbfO79Yk130_provenance.
- NP976963.RAyP3rmhDqMGYiWanXHFAP3wfGrM0Xx_4N74zxbfO79Yk130_assertion wasDerivedFrom befree-20150227 NP976963.RAyP3rmhDqMGYiWanXHFAP3wfGrM0Xx_4N74zxbfO79Yk130_provenance.
- NP976963.RAyP3rmhDqMGYiWanXHFAP3wfGrM0Xx_4N74zxbfO79Yk130_assertion wasGeneratedBy ECO_0000203 NP976963.RAyP3rmhDqMGYiWanXHFAP3wfGrM0Xx_4N74zxbfO79Yk130_provenance.
- befree-20150227 importedOn "2015-02-27" NP976963.RAyP3rmhDqMGYiWanXHFAP3wfGrM0Xx_4N74zxbfO79Yk130_provenance.