Matches in Nanopublications for { ?s ?p "[Range of the clinical phenotype caused by GCK mutations varies from complete insulin deficiency to extreme hyperinsulinemia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ?g. }
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- NP137315.RAsJYu50G3j7mipsEjK6bBy4IEWqsB5esjfHX-T3a-WdI130_assertion description "[Range of the clinical phenotype caused by GCK mutations varies from complete insulin deficiency to extreme hyperinsulinemia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP137315.RAsJYu50G3j7mipsEjK6bBy4IEWqsB5esjfHX-T3a-WdI130_provenance.
- assertion description "[Range of the clinical phenotype caused by GCK mutations varies from complete insulin deficiency to extreme hyperinsulinemia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
- NP200465.RA40t_rN-5SwS9Jn8Lf0Q9iA4dVRblVH3l5W5jHUWjrxk130_assertion description "[Range of the clinical phenotype caused by GCK mutations varies from complete insulin deficiency to extreme hyperinsulinemia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP200465.RA40t_rN-5SwS9Jn8Lf0Q9iA4dVRblVH3l5W5jHUWjrxk130_provenance.
- NP206085.RAFqE04Jp_KgnJ2UgLY56cfMjauxVRr1BiEVuMN9yvtN0130_assertion description "[Range of the clinical phenotype caused by GCK mutations varies from complete insulin deficiency to extreme hyperinsulinemia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP206085.RAFqE04Jp_KgnJ2UgLY56cfMjauxVRr1BiEVuMN9yvtN0130_provenance.