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- NP698543.RAd5cbLZZkHrOrUpezd1Dl5Y5S3zFiM5vi92vG4dHXQQ8130_assertion type Assertion NP698543.RAd5cbLZZkHrOrUpezd1Dl5Y5S3zFiM5vi92vG4dHXQQ8130_head.
- NP698543.RAd5cbLZZkHrOrUpezd1Dl5Y5S3zFiM5vi92vG4dHXQQ8130_assertion wasGeneratedBy ECO_0000203 NP698543.RAd5cbLZZkHrOrUpezd1Dl5Y5S3zFiM5vi92vG4dHXQQ8130_provenance.
- NP698543.RAd5cbLZZkHrOrUpezd1Dl5Y5S3zFiM5vi92vG4dHXQQ8130_assertion wasDerivedFrom befree-20140225 NP698543.RAd5cbLZZkHrOrUpezd1Dl5Y5S3zFiM5vi92vG4dHXQQ8130_provenance.
- NP698543.RAd5cbLZZkHrOrUpezd1Dl5Y5S3zFiM5vi92vG4dHXQQ8130_assertion SIO_000772 22876555 NP698543.RAd5cbLZZkHrOrUpezd1Dl5Y5S3zFiM5vi92vG4dHXQQ8130_provenance.
- NP698543.RAd5cbLZZkHrOrUpezd1Dl5Y5S3zFiM5vi92vG4dHXQQ8130_assertion evidence source_evidence_literature NP698543.RAd5cbLZZkHrOrUpezd1Dl5Y5S3zFiM5vi92vG4dHXQQ8130_provenance.
- NP698543.RAd5cbLZZkHrOrUpezd1Dl5Y5S3zFiM5vi92vG4dHXQQ8130_assertion description "[We report a girl with congenital hyperinsulinism due to novel homozygous mutation (c.2041-25 G>A; aberrant splicing mutation) in the ABCC8 gene encoding SUR1 and during somatostatin analog (octreotide) discontinuation developed by nonhypoglycemic seizures.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP698543.RAd5cbLZZkHrOrUpezd1Dl5Y5S3zFiM5vi92vG4dHXQQ8130_provenance.