Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP596248.RAWKhIHejlnUSgeiJxMwmcIKFP2sR6Ba0RDzRaTIixGWQ130_assertion> ?p ?o ?g. }
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- NP596248.RAWKhIHejlnUSgeiJxMwmcIKFP2sR6Ba0RDzRaTIixGWQ130_assertion type Assertion NP596248.RAWKhIHejlnUSgeiJxMwmcIKFP2sR6Ba0RDzRaTIixGWQ130_head.
- NP596248.RAWKhIHejlnUSgeiJxMwmcIKFP2sR6Ba0RDzRaTIixGWQ130_assertion description "[In summary, although heterozygous loss-of- function mutations in AKT2 can cause a syndrome of severe insulin resistance and lipodystrophy in humans, such mutations are uncommon causes of these syndromes.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP596248.RAWKhIHejlnUSgeiJxMwmcIKFP2sR6Ba0RDzRaTIixGWQ130_provenance.
- NP596248.RAWKhIHejlnUSgeiJxMwmcIKFP2sR6Ba0RDzRaTIixGWQ130_assertion evidence source_evidence_literature NP596248.RAWKhIHejlnUSgeiJxMwmcIKFP2sR6Ba0RDzRaTIixGWQ130_provenance.
- NP596248.RAWKhIHejlnUSgeiJxMwmcIKFP2sR6Ba0RDzRaTIixGWQ130_assertion SIO_000772 17327441 NP596248.RAWKhIHejlnUSgeiJxMwmcIKFP2sR6Ba0RDzRaTIixGWQ130_provenance.
- NP596248.RAWKhIHejlnUSgeiJxMwmcIKFP2sR6Ba0RDzRaTIixGWQ130_assertion wasDerivedFrom befree-2016 NP596248.RAWKhIHejlnUSgeiJxMwmcIKFP2sR6Ba0RDzRaTIixGWQ130_provenance.
- NP596248.RAWKhIHejlnUSgeiJxMwmcIKFP2sR6Ba0RDzRaTIixGWQ130_assertion wasGeneratedBy ECO_0000203 NP596248.RAWKhIHejlnUSgeiJxMwmcIKFP2sR6Ba0RDzRaTIixGWQ130_provenance.