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- NP337485.RAkzTW2_qeOgtORM8JJT2f8uOP_Owndv5SYaxshH49_Dc130_assertion type Assertion NP337485.RAkzTW2_qeOgtORM8JJT2f8uOP_Owndv5SYaxshH49_Dc130_head.
- NP337485.RAkzTW2_qeOgtORM8JJT2f8uOP_Owndv5SYaxshH49_Dc130_assertion wasGeneratedBy ECO_0000203 NP337485.RAkzTW2_qeOgtORM8JJT2f8uOP_Owndv5SYaxshH49_Dc130_provenance.
- NP337485.RAkzTW2_qeOgtORM8JJT2f8uOP_Owndv5SYaxshH49_Dc130_assertion wasDerivedFrom befree-2016 NP337485.RAkzTW2_qeOgtORM8JJT2f8uOP_Owndv5SYaxshH49_Dc130_provenance.
- NP337485.RAkzTW2_qeOgtORM8JJT2f8uOP_Owndv5SYaxshH49_Dc130_assertion SIO_000772 11723059 NP337485.RAkzTW2_qeOgtORM8JJT2f8uOP_Owndv5SYaxshH49_Dc130_provenance.
- NP337485.RAkzTW2_qeOgtORM8JJT2f8uOP_Owndv5SYaxshH49_Dc130_assertion evidence source_evidence_literature NP337485.RAkzTW2_qeOgtORM8JJT2f8uOP_Owndv5SYaxshH49_Dc130_provenance.
- NP337485.RAkzTW2_qeOgtORM8JJT2f8uOP_Owndv5SYaxshH49_Dc130_assertion description "[Most cases of hyperinsulinism of infancy (HI) are caused by mutations in either the sulfonylurea receptor-1 (SUR1) or the inward rectifying K(+) channel Kir6.2, two subunits of the beta-cell ATP-sensitive K(+) channel (K(ATP) channel).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP337485.RAkzTW2_qeOgtORM8JJT2f8uOP_Owndv5SYaxshH49_Dc130_provenance.