Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP433892.RAskLl0BVzT2rWu3GEGF7kyKdYV2DsIUGbgoj3NAYk21s130_assertion> ?p ?o ?g. }
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- NP433892.RAskLl0BVzT2rWu3GEGF7kyKdYV2DsIUGbgoj3NAYk21s130_assertion type Assertion NP433892.RAskLl0BVzT2rWu3GEGF7kyKdYV2DsIUGbgoj3NAYk21s130_head.
- NP433892.RAskLl0BVzT2rWu3GEGF7kyKdYV2DsIUGbgoj3NAYk21s130_assertion description "[K(ATP) channel mutations were most common (15%) followed by GLUD1 mutations causing hyperinsulinism with hyperammonemia (5.9%), and HNF4A mutations (5%).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP433892.RAskLl0BVzT2rWu3GEGF7kyKdYV2DsIUGbgoj3NAYk21s130_provenance.
- NP433892.RAskLl0BVzT2rWu3GEGF7kyKdYV2DsIUGbgoj3NAYk21s130_assertion evidence source_evidence_literature NP433892.RAskLl0BVzT2rWu3GEGF7kyKdYV2DsIUGbgoj3NAYk21s130_provenance.
- NP433892.RAskLl0BVzT2rWu3GEGF7kyKdYV2DsIUGbgoj3NAYk21s130_assertion SIO_000772 20164212 NP433892.RAskLl0BVzT2rWu3GEGF7kyKdYV2DsIUGbgoj3NAYk21s130_provenance.
- NP433892.RAskLl0BVzT2rWu3GEGF7kyKdYV2DsIUGbgoj3NAYk21s130_assertion wasDerivedFrom befree-20150227 NP433892.RAskLl0BVzT2rWu3GEGF7kyKdYV2DsIUGbgoj3NAYk21s130_provenance.
- NP433892.RAskLl0BVzT2rWu3GEGF7kyKdYV2DsIUGbgoj3NAYk21s130_assertion wasGeneratedBy ECO_0000203 NP433892.RAskLl0BVzT2rWu3GEGF7kyKdYV2DsIUGbgoj3NAYk21s130_provenance.