Matches in Nanopublications for { ?s ?p "[Monogenic forms of T2DM with profound defect in insulin secretion include subtypes of maturity onset diabetes of the young (MODY), maternally inherited diabetes with deafness (MIDD) caused by mitochondrial mutations, and rare cases resulting from insulin gene mutations.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ?g. }
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- NP492433.RAntoJ6aOA-1MOidlt9gyJFUWhlEb46ftn1pLq080K_sA130_assertion description "[Monogenic forms of T2DM with profound defect in insulin secretion include subtypes of maturity onset diabetes of the young (MODY), maternally inherited diabetes with deafness (MIDD) caused by mitochondrial mutations, and rare cases resulting from insulin gene mutations.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP492433.RAntoJ6aOA-1MOidlt9gyJFUWhlEb46ftn1pLq080K_sA130_provenance.
- NP594843.RAjPZefrfXFzfzSB0I8mHC4VlW4SVinMO_C3ntjH7OrIg130_assertion description "[Monogenic forms of T2DM with profound defect in insulin secretion include subtypes of maturity onset diabetes of the young (MODY), maternally inherited diabetes with deafness (MIDD) caused by mitochondrial mutations, and rare cases resulting from insulin gene mutations.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP594843.RAjPZefrfXFzfzSB0I8mHC4VlW4SVinMO_C3ntjH7OrIg130_provenance.
- NP677425.RA3SyDdTABctAjEVQZvLtN2arJ3Ibgih5NtMJcE0tFSVQ130_assertion description "[Monogenic forms of T2DM with profound defect in insulin secretion include subtypes of maturity onset diabetes of the young (MODY), maternally inherited diabetes with deafness (MIDD) caused by mitochondrial mutations, and rare cases resulting from insulin gene mutations.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP677425.RA3SyDdTABctAjEVQZvLtN2arJ3Ibgih5NtMJcE0tFSVQ130_provenance.
- NP499387.RA1tfH9SSQpEJ4aN0jjyYUexFohRnf-PiDuoK8-oVYOM0130_assertion description "[Monogenic forms of T2DM with profound defect in insulin secretion include subtypes of maturity onset diabetes of the young (MODY), maternally inherited diabetes with deafness (MIDD) caused by mitochondrial mutations, and rare cases resulting from insulin gene mutations.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP499387.RA1tfH9SSQpEJ4aN0jjyYUexFohRnf-PiDuoK8-oVYOM0130_provenance.