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- NP445604.RA43kQ0-QWKAhcG5-GpnPiQPIhy-GYpJIBbAu7JaLdEXA130_assertion type Assertion NP445604.RA43kQ0-QWKAhcG5-GpnPiQPIhy-GYpJIBbAu7JaLdEXA130_head.
- NP445604.RA43kQ0-QWKAhcG5-GpnPiQPIhy-GYpJIBbAu7JaLdEXA130_assertion wasGeneratedBy ECO_0000203 NP445604.RA43kQ0-QWKAhcG5-GpnPiQPIhy-GYpJIBbAu7JaLdEXA130_provenance.
- NP445604.RA43kQ0-QWKAhcG5-GpnPiQPIhy-GYpJIBbAu7JaLdEXA130_assertion wasDerivedFrom befree-2016 NP445604.RA43kQ0-QWKAhcG5-GpnPiQPIhy-GYpJIBbAu7JaLdEXA130_provenance.
- NP445604.RA43kQ0-QWKAhcG5-GpnPiQPIhy-GYpJIBbAu7JaLdEXA130_assertion SIO_000772 15161766 NP445604.RA43kQ0-QWKAhcG5-GpnPiQPIhy-GYpJIBbAu7JaLdEXA130_provenance.
- NP445604.RA43kQ0-QWKAhcG5-GpnPiQPIhy-GYpJIBbAu7JaLdEXA130_assertion evidence source_evidence_literature NP445604.RA43kQ0-QWKAhcG5-GpnPiQPIhy-GYpJIBbAu7JaLdEXA130_provenance.
- NP445604.RA43kQ0-QWKAhcG5-GpnPiQPIhy-GYpJIBbAu7JaLdEXA130_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." NP445604.RA43kQ0-QWKAhcG5-GpnPiQPIhy-GYpJIBbAu7JaLdEXA130_provenance.