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- NP211101.RAty5b4aNAvb_p9jku_6FPB03OivDCRNX35wP6UXAD23Y130_assertion type Assertion NP211101.RAty5b4aNAvb_p9jku_6FPB03OivDCRNX35wP6UXAD23Y130_head.
- NP211101.RAty5b4aNAvb_p9jku_6FPB03OivDCRNX35wP6UXAD23Y130_assertion wasGeneratedBy ECO_0000203 NP211101.RAty5b4aNAvb_p9jku_6FPB03OivDCRNX35wP6UXAD23Y130_provenance.
- NP211101.RAty5b4aNAvb_p9jku_6FPB03OivDCRNX35wP6UXAD23Y130_assertion wasDerivedFrom lhgdn-20090331 NP211101.RAty5b4aNAvb_p9jku_6FPB03OivDCRNX35wP6UXAD23Y130_provenance.
- NP211101.RAty5b4aNAvb_p9jku_6FPB03OivDCRNX35wP6UXAD23Y130_assertion SIO_000772 16332676 NP211101.RAty5b4aNAvb_p9jku_6FPB03OivDCRNX35wP6UXAD23Y130_provenance.
- NP211101.RAty5b4aNAvb_p9jku_6FPB03OivDCRNX35wP6UXAD23Y130_assertion evidence source_evidence_literature NP211101.RAty5b4aNAvb_p9jku_6FPB03OivDCRNX35wP6UXAD23Y130_provenance.
- NP211101.RAty5b4aNAvb_p9jku_6FPB03OivDCRNX35wP6UXAD23Y130_assertion description "[identification of a novel KCNJ11 mutation associated with congenital hyperinsulinism that renders a missense mutation, F55L, in the Kir6.2 protein.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP211101.RAty5b4aNAvb_p9jku_6FPB03OivDCRNX35wP6UXAD23Y130_provenance.