Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP912793.RAryiwZHkcBvGcjHQIO-ieUYaag4LUuwseMyFmB_DBp2Y130_assertion> ?p ?o ?g. }
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- NP912793.RAryiwZHkcBvGcjHQIO-ieUYaag4LUuwseMyFmB_DBp2Y130_assertion type Assertion NP912793.RAryiwZHkcBvGcjHQIO-ieUYaag4LUuwseMyFmB_DBp2Y130_head.
- NP912793.RAryiwZHkcBvGcjHQIO-ieUYaag4LUuwseMyFmB_DBp2Y130_assertion description "[We demonstrate that the mutation S100P is associated with proteasome-mediated degradation, and thus presumably represents a null mutation comparable to the Ca8 mutation underlying the previously described waddles mouse, which exhibits ataxia and appendicular dystonia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP912793.RAryiwZHkcBvGcjHQIO-ieUYaag4LUuwseMyFmB_DBp2Y130_provenance.
- NP912793.RAryiwZHkcBvGcjHQIO-ieUYaag4LUuwseMyFmB_DBp2Y130_assertion evidence source_evidence_literature NP912793.RAryiwZHkcBvGcjHQIO-ieUYaag4LUuwseMyFmB_DBp2Y130_provenance.
- NP912793.RAryiwZHkcBvGcjHQIO-ieUYaag4LUuwseMyFmB_DBp2Y130_assertion SIO_000772 19461874 NP912793.RAryiwZHkcBvGcjHQIO-ieUYaag4LUuwseMyFmB_DBp2Y130_provenance.
- NP912793.RAryiwZHkcBvGcjHQIO-ieUYaag4LUuwseMyFmB_DBp2Y130_assertion wasDerivedFrom befree-20140225 NP912793.RAryiwZHkcBvGcjHQIO-ieUYaag4LUuwseMyFmB_DBp2Y130_provenance.
- NP912793.RAryiwZHkcBvGcjHQIO-ieUYaag4LUuwseMyFmB_DBp2Y130_assertion wasGeneratedBy ECO_0000203 NP912793.RAryiwZHkcBvGcjHQIO-ieUYaag4LUuwseMyFmB_DBp2Y130_provenance.