Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP585192.RACQulIhS2GTw8on2-g8s6Im-78QMahjvx5uungp5V_gI130_assertion> ?p ?o ?g. }
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- NP585192.RACQulIhS2GTw8on2-g8s6Im-78QMahjvx5uungp5V_gI130_assertion type Assertion NP585192.RACQulIhS2GTw8on2-g8s6Im-78QMahjvx5uungp5V_gI130_head.
- NP585192.RACQulIhS2GTw8on2-g8s6Im-78QMahjvx5uungp5V_gI130_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." NP585192.RACQulIhS2GTw8on2-g8s6Im-78QMahjvx5uungp5V_gI130_provenance.
- NP585192.RACQulIhS2GTw8on2-g8s6Im-78QMahjvx5uungp5V_gI130_assertion evidence source_evidence_literature NP585192.RACQulIhS2GTw8on2-g8s6Im-78QMahjvx5uungp5V_gI130_provenance.
- NP585192.RACQulIhS2GTw8on2-g8s6Im-78QMahjvx5uungp5V_gI130_assertion SIO_000772 19461874 NP585192.RACQulIhS2GTw8on2-g8s6Im-78QMahjvx5uungp5V_gI130_provenance.
- NP585192.RACQulIhS2GTw8on2-g8s6Im-78QMahjvx5uungp5V_gI130_assertion wasDerivedFrom befree-20140225 NP585192.RACQulIhS2GTw8on2-g8s6Im-78QMahjvx5uungp5V_gI130_provenance.
- NP585192.RACQulIhS2GTw8on2-g8s6Im-78QMahjvx5uungp5V_gI130_assertion wasGeneratedBy ECO_0000203 NP585192.RACQulIhS2GTw8on2-g8s6Im-78QMahjvx5uungp5V_gI130_provenance.