Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP138084.RAGZnicm9zMLtK4RjBnwrrWcCRFLTIk-W716NCrX8MGZI130_assertion> ?p ?o ?g. }
Showing items 1 to 6 of
6
with 100 items per page.
- NP138084.RAGZnicm9zMLtK4RjBnwrrWcCRFLTIk-W716NCrX8MGZI130_assertion type Assertion NP138084.RAGZnicm9zMLtK4RjBnwrrWcCRFLTIk-W716NCrX8MGZI130_head.
- NP138084.RAGZnicm9zMLtK4RjBnwrrWcCRFLTIk-W716NCrX8MGZI130_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." NP138084.RAGZnicm9zMLtK4RjBnwrrWcCRFLTIk-W716NCrX8MGZI130_provenance.
- NP138084.RAGZnicm9zMLtK4RjBnwrrWcCRFLTIk-W716NCrX8MGZI130_assertion evidence source_evidence_literature NP138084.RAGZnicm9zMLtK4RjBnwrrWcCRFLTIk-W716NCrX8MGZI130_provenance.
- NP138084.RAGZnicm9zMLtK4RjBnwrrWcCRFLTIk-W716NCrX8MGZI130_assertion SIO_000772 20164212 NP138084.RAGZnicm9zMLtK4RjBnwrrWcCRFLTIk-W716NCrX8MGZI130_provenance.
- NP138084.RAGZnicm9zMLtK4RjBnwrrWcCRFLTIk-W716NCrX8MGZI130_assertion wasDerivedFrom gad-20150221 NP138084.RAGZnicm9zMLtK4RjBnwrrWcCRFLTIk-W716NCrX8MGZI130_provenance.
- NP138084.RAGZnicm9zMLtK4RjBnwrrWcCRFLTIk-W716NCrX8MGZI130_assertion wasGeneratedBy ECO_0000203 NP138084.RAGZnicm9zMLtK4RjBnwrrWcCRFLTIk-W716NCrX8MGZI130_provenance.