Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP220195.RAXHwqAhgTmCea5kDjRMI6P0mtseLY74speHLr0FWK6mU130_assertion> ?p ?o ?g. }
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- NP220195.RAXHwqAhgTmCea5kDjRMI6P0mtseLY74speHLr0FWK6mU130_assertion type Assertion NP220195.RAXHwqAhgTmCea5kDjRMI6P0mtseLY74speHLr0FWK6mU130_head.
- NP220195.RAXHwqAhgTmCea5kDjRMI6P0mtseLY74speHLr0FWK6mU130_assertion wasGeneratedBy ECO_0000203 NP220195.RAXHwqAhgTmCea5kDjRMI6P0mtseLY74speHLr0FWK6mU130_provenance.
- NP220195.RAXHwqAhgTmCea5kDjRMI6P0mtseLY74speHLr0FWK6mU130_assertion wasDerivedFrom befree-20140225 NP220195.RAXHwqAhgTmCea5kDjRMI6P0mtseLY74speHLr0FWK6mU130_provenance.
- NP220195.RAXHwqAhgTmCea5kDjRMI6P0mtseLY74speHLr0FWK6mU130_assertion SIO_000772 11723059 NP220195.RAXHwqAhgTmCea5kDjRMI6P0mtseLY74speHLr0FWK6mU130_provenance.
- NP220195.RAXHwqAhgTmCea5kDjRMI6P0mtseLY74speHLr0FWK6mU130_assertion evidence source_evidence_literature NP220195.RAXHwqAhgTmCea5kDjRMI6P0mtseLY74speHLr0FWK6mU130_provenance.
- NP220195.RAXHwqAhgTmCea5kDjRMI6P0mtseLY74speHLr0FWK6mU130_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." NP220195.RAXHwqAhgTmCea5kDjRMI6P0mtseLY74speHLr0FWK6mU130_provenance.