Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP642895.RAbvyjWl-4abhSKibb3jb3wyM4ynYjWMF2xNDCr7b9t6U130_assertion> ?p ?o ?g. }
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- NP642895.RAbvyjWl-4abhSKibb3jb3wyM4ynYjWMF2xNDCr7b9t6U130_assertion type Assertion NP642895.RAbvyjWl-4abhSKibb3jb3wyM4ynYjWMF2xNDCr7b9t6U130_head.
- NP642895.RAbvyjWl-4abhSKibb3jb3wyM4ynYjWMF2xNDCr7b9t6U130_assertion description "[Several missense mutations in the protein kinase C? (?PKC) gene have been found to cause spinocerebellar ataxia type 14 (SCA14), an autosomal dominant neurodegenerative disease.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP642895.RAbvyjWl-4abhSKibb3jb3wyM4ynYjWMF2xNDCr7b9t6U130_provenance.
- NP642895.RAbvyjWl-4abhSKibb3jb3wyM4ynYjWMF2xNDCr7b9t6U130_assertion evidence source_evidence_literature NP642895.RAbvyjWl-4abhSKibb3jb3wyM4ynYjWMF2xNDCr7b9t6U130_provenance.
- NP642895.RAbvyjWl-4abhSKibb3jb3wyM4ynYjWMF2xNDCr7b9t6U130_assertion SIO_000772 20938103 NP642895.RAbvyjWl-4abhSKibb3jb3wyM4ynYjWMF2xNDCr7b9t6U130_provenance.
- NP642895.RAbvyjWl-4abhSKibb3jb3wyM4ynYjWMF2xNDCr7b9t6U130_assertion wasDerivedFrom befree-20150227 NP642895.RAbvyjWl-4abhSKibb3jb3wyM4ynYjWMF2xNDCr7b9t6U130_provenance.
- NP642895.RAbvyjWl-4abhSKibb3jb3wyM4ynYjWMF2xNDCr7b9t6U130_assertion wasGeneratedBy ECO_0000203 NP642895.RAbvyjWl-4abhSKibb3jb3wyM4ynYjWMF2xNDCr7b9t6U130_provenance.