Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP397608.RAwTE6G4QKn-65kOEaE_Xbz2ONR5uGcG5aGggxiXDXk9w130_assertion> ?p ?o ?g. }
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- NP397608.RAwTE6G4QKn-65kOEaE_Xbz2ONR5uGcG5aGggxiXDXk9w130_assertion type Assertion NP397608.RAwTE6G4QKn-65kOEaE_Xbz2ONR5uGcG5aGggxiXDXk9w130_head.
- NP397608.RAwTE6G4QKn-65kOEaE_Xbz2ONR5uGcG5aGggxiXDXk9w130_assertion description "[Mutations that truncate the C-terminal non-catalytic moiety of TTBK2 (tau tubulin kinase 2) cause the inherited, autosomal dominant, SCA11 (spinocerebellar ataxia type�11) movement disorder.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP397608.RAwTE6G4QKn-65kOEaE_Xbz2ONR5uGcG5aGggxiXDXk9w130_provenance.
- NP397608.RAwTE6G4QKn-65kOEaE_Xbz2ONR5uGcG5aGggxiXDXk9w130_assertion evidence source_evidence_literature NP397608.RAwTE6G4QKn-65kOEaE_Xbz2ONR5uGcG5aGggxiXDXk9w130_provenance.
- NP397608.RAwTE6G4QKn-65kOEaE_Xbz2ONR5uGcG5aGggxiXDXk9w130_assertion SIO_000772 21548880 NP397608.RAwTE6G4QKn-65kOEaE_Xbz2ONR5uGcG5aGggxiXDXk9w130_provenance.
- NP397608.RAwTE6G4QKn-65kOEaE_Xbz2ONR5uGcG5aGggxiXDXk9w130_assertion wasDerivedFrom befree-20140225 NP397608.RAwTE6G4QKn-65kOEaE_Xbz2ONR5uGcG5aGggxiXDXk9w130_provenance.
- NP397608.RAwTE6G4QKn-65kOEaE_Xbz2ONR5uGcG5aGggxiXDXk9w130_assertion wasGeneratedBy ECO_0000203 NP397608.RAwTE6G4QKn-65kOEaE_Xbz2ONR5uGcG5aGggxiXDXk9w130_provenance.