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- NP453475.RA0nOSBUhMsUvBmafukqOCK7xe7rxjmXKJlEiNmoqOZbA130_assertion type Assertion NP453475.RA0nOSBUhMsUvBmafukqOCK7xe7rxjmXKJlEiNmoqOZbA130_head.
- NP453475.RA0nOSBUhMsUvBmafukqOCK7xe7rxjmXKJlEiNmoqOZbA130_assertion description "[These findings demonstrate that the range of the clinical phenotype caused by GCK mutations varies from complete insulin deficiency to extreme hyperinsulinemia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP453475.RA0nOSBUhMsUvBmafukqOCK7xe7rxjmXKJlEiNmoqOZbA130_provenance.
- NP453475.RA0nOSBUhMsUvBmafukqOCK7xe7rxjmXKJlEiNmoqOZbA130_assertion evidence source_evidence_literature NP453475.RA0nOSBUhMsUvBmafukqOCK7xe7rxjmXKJlEiNmoqOZbA130_provenance.
- NP453475.RA0nOSBUhMsUvBmafukqOCK7xe7rxjmXKJlEiNmoqOZbA130_assertion SIO_000772 15277402 NP453475.RA0nOSBUhMsUvBmafukqOCK7xe7rxjmXKJlEiNmoqOZbA130_provenance.
- NP453475.RA0nOSBUhMsUvBmafukqOCK7xe7rxjmXKJlEiNmoqOZbA130_assertion wasDerivedFrom befree-2016 NP453475.RA0nOSBUhMsUvBmafukqOCK7xe7rxjmXKJlEiNmoqOZbA130_provenance.
- NP453475.RA0nOSBUhMsUvBmafukqOCK7xe7rxjmXKJlEiNmoqOZbA130_assertion wasGeneratedBy ECO_0000203 NP453475.RA0nOSBUhMsUvBmafukqOCK7xe7rxjmXKJlEiNmoqOZbA130_provenance.