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- NP796985.RA1qPIWDrBKbwMUFxWzKurHcyRDfHMb_W86yFgF6KU-Ac130_assertion type Assertion NP796985.RA1qPIWDrBKbwMUFxWzKurHcyRDfHMb_W86yFgF6KU-Ac130_head.
- NP796985.RA1qPIWDrBKbwMUFxWzKurHcyRDfHMb_W86yFgF6KU-Ac130_assertion wasGeneratedBy ECO_0000203 NP796985.RA1qPIWDrBKbwMUFxWzKurHcyRDfHMb_W86yFgF6KU-Ac130_provenance.
- NP796985.RA1qPIWDrBKbwMUFxWzKurHcyRDfHMb_W86yFgF6KU-Ac130_assertion wasDerivedFrom befree-20150227 NP796985.RA1qPIWDrBKbwMUFxWzKurHcyRDfHMb_W86yFgF6KU-Ac130_provenance.
- NP796985.RA1qPIWDrBKbwMUFxWzKurHcyRDfHMb_W86yFgF6KU-Ac130_assertion SIO_000772 19146401 NP796985.RA1qPIWDrBKbwMUFxWzKurHcyRDfHMb_W86yFgF6KU-Ac130_provenance.
- NP796985.RA1qPIWDrBKbwMUFxWzKurHcyRDfHMb_W86yFgF6KU-Ac130_assertion evidence source_evidence_literature NP796985.RA1qPIWDrBKbwMUFxWzKurHcyRDfHMb_W86yFgF6KU-Ac130_provenance.
- NP796985.RA1qPIWDrBKbwMUFxWzKurHcyRDfHMb_W86yFgF6KU-Ac130_assertion description "[We describe the discovery of 11 new activating mutations in the human glk gene associated with the disease persistent hyperinsulinemic hypoglycemia of infancy (PHHI).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP796985.RA1qPIWDrBKbwMUFxWzKurHcyRDfHMb_W86yFgF6KU-Ac130_provenance.