Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP680113.RAHAMXNz6WDksHzopLKarppx1MpeW6l7sy3Ml0Yb1kNKE130_assertion> ?p ?o ?g. }
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- NP680113.RAHAMXNz6WDksHzopLKarppx1MpeW6l7sy3Ml0Yb1kNKE130_assertion type Assertion NP680113.RAHAMXNz6WDksHzopLKarppx1MpeW6l7sy3Ml0Yb1kNKE130_head.
- NP680113.RAHAMXNz6WDksHzopLKarppx1MpeW6l7sy3Ml0Yb1kNKE130_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." NP680113.RAHAMXNz6WDksHzopLKarppx1MpeW6l7sy3Ml0Yb1kNKE130_provenance.
- NP680113.RAHAMXNz6WDksHzopLKarppx1MpeW6l7sy3Ml0Yb1kNKE130_assertion evidence source_evidence_literature NP680113.RAHAMXNz6WDksHzopLKarppx1MpeW6l7sy3Ml0Yb1kNKE130_provenance.
- NP680113.RAHAMXNz6WDksHzopLKarppx1MpeW6l7sy3Ml0Yb1kNKE130_assertion SIO_000772 19461874 NP680113.RAHAMXNz6WDksHzopLKarppx1MpeW6l7sy3Ml0Yb1kNKE130_provenance.
- NP680113.RAHAMXNz6WDksHzopLKarppx1MpeW6l7sy3Ml0Yb1kNKE130_assertion wasDerivedFrom befree-20150227 NP680113.RAHAMXNz6WDksHzopLKarppx1MpeW6l7sy3Ml0Yb1kNKE130_provenance.
- NP680113.RAHAMXNz6WDksHzopLKarppx1MpeW6l7sy3Ml0Yb1kNKE130_assertion wasGeneratedBy ECO_0000203 NP680113.RAHAMXNz6WDksHzopLKarppx1MpeW6l7sy3Ml0Yb1kNKE130_provenance.