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- NP513648.RAkdAmvgo4tdkj3csEz1EU1_q0e-XZxlkqQmMO-Y6J7B4130_assertion type Assertion NP513648.RAkdAmvgo4tdkj3csEz1EU1_q0e-XZxlkqQmMO-Y6J7B4130_head.
- NP513648.RAkdAmvgo4tdkj3csEz1EU1_q0e-XZxlkqQmMO-Y6J7B4130_assertion wasGeneratedBy ECO_0000203 NP513648.RAkdAmvgo4tdkj3csEz1EU1_q0e-XZxlkqQmMO-Y6J7B4130_provenance.
- NP513648.RAkdAmvgo4tdkj3csEz1EU1_q0e-XZxlkqQmMO-Y6J7B4130_assertion wasDerivedFrom befree-20150227 NP513648.RAkdAmvgo4tdkj3csEz1EU1_q0e-XZxlkqQmMO-Y6J7B4130_provenance.
- NP513648.RAkdAmvgo4tdkj3csEz1EU1_q0e-XZxlkqQmMO-Y6J7B4130_assertion SIO_000772 15161766 NP513648.RAkdAmvgo4tdkj3csEz1EU1_q0e-XZxlkqQmMO-Y6J7B4130_provenance.
- NP513648.RAkdAmvgo4tdkj3csEz1EU1_q0e-XZxlkqQmMO-Y6J7B4130_assertion evidence source_evidence_literature NP513648.RAkdAmvgo4tdkj3csEz1EU1_q0e-XZxlkqQmMO-Y6J7B4130_provenance.
- NP513648.RAkdAmvgo4tdkj3csEz1EU1_q0e-XZxlkqQmMO-Y6J7B4130_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." NP513648.RAkdAmvgo4tdkj3csEz1EU1_q0e-XZxlkqQmMO-Y6J7B4130_provenance.