Matches in Nanopublications for { ?s ?p "[These findings demonstrate that the 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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- NP718068.RArd_Qt6mUeVtJaRTgWJ2CkJHn_PybWJNp3eikYrgl8GA130_assertion description "[These findings demonstrate that the 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." NP718068.RArd_Qt6mUeVtJaRTgWJ2CkJHn_PybWJNp3eikYrgl8GA130_provenance.
- NP747016.RAfpunTUhWK5WhtD7Oimyr9xqv_g-vQnOi1HH0-o0vwxw130_assertion description "[These findings demonstrate that the 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." NP747016.RAfpunTUhWK5WhtD7Oimyr9xqv_g-vQnOi1HH0-o0vwxw130_provenance.
- NP453475.RA0nOSBUhMsUvBmafukqOCK7xe7rxjmXKJlEiNmoqOZbA130_assertion description "[These findings demonstrate that the 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." NP453475.RA0nOSBUhMsUvBmafukqOCK7xe7rxjmXKJlEiNmoqOZbA130_provenance.