Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP594843.RAjPZefrfXFzfzSB0I8mHC4VlW4SVinMO_C3ntjH7OrIg130_assertion> ?p ?o ?g. }
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- NP594843.RAjPZefrfXFzfzSB0I8mHC4VlW4SVinMO_C3ntjH7OrIg130_assertion type Assertion NP594843.RAjPZefrfXFzfzSB0I8mHC4VlW4SVinMO_C3ntjH7OrIg130_head.
- 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.
- NP594843.RAjPZefrfXFzfzSB0I8mHC4VlW4SVinMO_C3ntjH7OrIg130_assertion evidence source_evidence_literature NP594843.RAjPZefrfXFzfzSB0I8mHC4VlW4SVinMO_C3ntjH7OrIg130_provenance.
- NP594843.RAjPZefrfXFzfzSB0I8mHC4VlW4SVinMO_C3ntjH7OrIg130_assertion SIO_000772 15955369 NP594843.RAjPZefrfXFzfzSB0I8mHC4VlW4SVinMO_C3ntjH7OrIg130_provenance.
- NP594843.RAjPZefrfXFzfzSB0I8mHC4VlW4SVinMO_C3ntjH7OrIg130_assertion wasDerivedFrom befree-20140225 NP594843.RAjPZefrfXFzfzSB0I8mHC4VlW4SVinMO_C3ntjH7OrIg130_provenance.
- NP594843.RAjPZefrfXFzfzSB0I8mHC4VlW4SVinMO_C3ntjH7OrIg130_assertion wasGeneratedBy ECO_0000203 NP594843.RAjPZefrfXFzfzSB0I8mHC4VlW4SVinMO_C3ntjH7OrIg130_provenance.