Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP649639.RAbZ1YWWnVCJHNim9ba6uCuaNU30VkjwmnRcV1jaGrcMw130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP649639.RAbZ1YWWnVCJHNim9ba6uCuaNU30VkjwmnRcV1jaGrcMw130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP649639.RAbZ1YWWnVCJHNim9ba6uCuaNU30VkjwmnRcV1jaGrcMw130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP649639.RAbZ1YWWnVCJHNim9ba6uCuaNU30VkjwmnRcV1jaGrcMw130_provenance.
- befree-2016 importedOn "2016-02-19" NP649639.RAbZ1YWWnVCJHNim9ba6uCuaNU30VkjwmnRcV1jaGrcMw130_provenance.
- 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.