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- NP3471.RA7rcKJEszbbeVwin6wC8o3KSEnOmbjV4EgoVeEq3XOF0130_assertion type Assertion NP3471.RA7rcKJEszbbeVwin6wC8o3KSEnOmbjV4EgoVeEq3XOF0130_head.
- NP3471.RA7rcKJEszbbeVwin6wC8o3KSEnOmbjV4EgoVeEq3XOF0130_assertion wasGeneratedBy ECO_0000218 NP3471.RA7rcKJEszbbeVwin6wC8o3KSEnOmbjV4EgoVeEq3XOF0130_provenance.
- NP3471.RA7rcKJEszbbeVwin6wC8o3KSEnOmbjV4EgoVeEq3XOF0130_assertion wasDerivedFrom uniprot-2016 NP3471.RA7rcKJEszbbeVwin6wC8o3KSEnOmbjV4EgoVeEq3XOF0130_provenance.
- NP3471.RA7rcKJEszbbeVwin6wC8o3KSEnOmbjV4EgoVeEq3XOF0130_assertion SIO_000772 15161766 NP3471.RA7rcKJEszbbeVwin6wC8o3KSEnOmbjV4EgoVeEq3XOF0130_provenance.
- NP3471.RA7rcKJEszbbeVwin6wC8o3KSEnOmbjV4EgoVeEq3XOF0130_assertion evidence source_evidence_curated NP3471.RA7rcKJEszbbeVwin6wC8o3KSEnOmbjV4EgoVeEq3XOF0130_provenance.
- NP3471.RA7rcKJEszbbeVwin6wC8o3KSEnOmbjV4EgoVeEq3XOF0130_assertion description "[A novel syndrome of autosomal-dominant hyperinsulinemic hypoglycemia linked to a mutation in the human insulin receptor gene.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP3471.RA7rcKJEszbbeVwin6wC8o3KSEnOmbjV4EgoVeEq3XOF0130_provenance.