Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP1013338.RAVCdmvM0asDnZJLKDJRLRsZhLCQXFpVqJeK1ww-cVnmY130_assertion> ?p ?o ?g. }
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- NP1013338.RAVCdmvM0asDnZJLKDJRLRsZhLCQXFpVqJeK1ww-cVnmY130_assertion type Assertion NP1013338.RAVCdmvM0asDnZJLKDJRLRsZhLCQXFpVqJeK1ww-cVnmY130_head.
- NP1013338.RAVCdmvM0asDnZJLKDJRLRsZhLCQXFpVqJeK1ww-cVnmY130_assertion description "[This AIR pattern suggested a K(ATP) channel defect because it resembled that seen in children with recessive hyperinsulinism due to two common SUR1 mutations, g3992-9a and delPhe1388.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1013338.RAVCdmvM0asDnZJLKDJRLRsZhLCQXFpVqJeK1ww-cVnmY130_provenance.
- NP1013338.RAVCdmvM0asDnZJLKDJRLRsZhLCQXFpVqJeK1ww-cVnmY130_assertion evidence source_evidence_literature NP1013338.RAVCdmvM0asDnZJLKDJRLRsZhLCQXFpVqJeK1ww-cVnmY130_provenance.
- NP1013338.RAVCdmvM0asDnZJLKDJRLRsZhLCQXFpVqJeK1ww-cVnmY130_assertion SIO_000772 12941782 NP1013338.RAVCdmvM0asDnZJLKDJRLRsZhLCQXFpVqJeK1ww-cVnmY130_provenance.
- NP1013338.RAVCdmvM0asDnZJLKDJRLRsZhLCQXFpVqJeK1ww-cVnmY130_assertion wasDerivedFrom befree-20150227 NP1013338.RAVCdmvM0asDnZJLKDJRLRsZhLCQXFpVqJeK1ww-cVnmY130_provenance.
- NP1013338.RAVCdmvM0asDnZJLKDJRLRsZhLCQXFpVqJeK1ww-cVnmY130_assertion wasGeneratedBy ECO_0000203 NP1013338.RAVCdmvM0asDnZJLKDJRLRsZhLCQXFpVqJeK1ww-cVnmY130_provenance.