Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP522684.RAMCbO6_7G9vXjOFaNmKOVO-WLwIKO325HZnML7Dt0A-o130_assertion> ?p ?o ?g. }
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- NP522684.RAMCbO6_7G9vXjOFaNmKOVO-WLwIKO325HZnML7Dt0A-o130_assertion type Assertion NP522684.RAMCbO6_7G9vXjOFaNmKOVO-WLwIKO325HZnML7Dt0A-o130_head.
- NP522684.RAMCbO6_7G9vXjOFaNmKOVO-WLwIKO325HZnML7Dt0A-o130_assertion wasGeneratedBy ECO_0000203 NP522684.RAMCbO6_7G9vXjOFaNmKOVO-WLwIKO325HZnML7Dt0A-o130_provenance.
- NP522684.RAMCbO6_7G9vXjOFaNmKOVO-WLwIKO325HZnML7Dt0A-o130_assertion wasDerivedFrom befree-20150227 NP522684.RAMCbO6_7G9vXjOFaNmKOVO-WLwIKO325HZnML7Dt0A-o130_provenance.
- NP522684.RAMCbO6_7G9vXjOFaNmKOVO-WLwIKO325HZnML7Dt0A-o130_assertion SIO_000772 11723059 NP522684.RAMCbO6_7G9vXjOFaNmKOVO-WLwIKO325HZnML7Dt0A-o130_provenance.
- NP522684.RAMCbO6_7G9vXjOFaNmKOVO-WLwIKO325HZnML7Dt0A-o130_assertion evidence source_evidence_literature NP522684.RAMCbO6_7G9vXjOFaNmKOVO-WLwIKO325HZnML7Dt0A-o130_provenance.
- NP522684.RAMCbO6_7G9vXjOFaNmKOVO-WLwIKO325HZnML7Dt0A-o130_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." NP522684.RAMCbO6_7G9vXjOFaNmKOVO-WLwIKO325HZnML7Dt0A-o130_provenance.