Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP649639.RAbZ1YWWnVCJHNim9ba6uCuaNU30VkjwmnRcV1jaGrcMw130_assertion> ?p ?o ?g. }
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- NP649639.RAbZ1YWWnVCJHNim9ba6uCuaNU30VkjwmnRcV1jaGrcMw130_assertion type Assertion NP649639.RAbZ1YWWnVCJHNim9ba6uCuaNU30VkjwmnRcV1jaGrcMw130_head.
- NP649639.RAbZ1YWWnVCJHNim9ba6uCuaNU30VkjwmnRcV1jaGrcMw130_assertion wasGeneratedBy ECO_0000203 NP649639.RAbZ1YWWnVCJHNim9ba6uCuaNU30VkjwmnRcV1jaGrcMw130_provenance.
- NP649639.RAbZ1YWWnVCJHNim9ba6uCuaNU30VkjwmnRcV1jaGrcMw130_assertion wasDerivedFrom befree-2016 NP649639.RAbZ1YWWnVCJHNim9ba6uCuaNU30VkjwmnRcV1jaGrcMw130_provenance.
- NP649639.RAbZ1YWWnVCJHNim9ba6uCuaNU30VkjwmnRcV1jaGrcMw130_assertion SIO_000772 18192540 NP649639.RAbZ1YWWnVCJHNim9ba6uCuaNU30VkjwmnRcV1jaGrcMw130_provenance.
- NP649639.RAbZ1YWWnVCJHNim9ba6uCuaNU30VkjwmnRcV1jaGrcMw130_assertion evidence source_evidence_literature NP649639.RAbZ1YWWnVCJHNim9ba6uCuaNU30VkjwmnRcV1jaGrcMw130_provenance.
- NP649639.RAbZ1YWWnVCJHNim9ba6uCuaNU30VkjwmnRcV1jaGrcMw130_assertion description "[Our findings extend the phenotype of INS mutation carriers and suggest that INS screening is warranted not only in neonatal diabetes, but also in MODY and in selected cases of type 1 diabetes.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP649639.RAbZ1YWWnVCJHNim9ba6uCuaNU30VkjwmnRcV1jaGrcMw130_provenance.