Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP681606.RAHL6MBiqBGzc0vpUp5KUiRRVOhjMhnVp6wcM5WX0SYfE130_assertion> ?p ?o ?g. }
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- NP681606.RAHL6MBiqBGzc0vpUp5KUiRRVOhjMhnVp6wcM5WX0SYfE130_assertion type Assertion NP681606.RAHL6MBiqBGzc0vpUp5KUiRRVOhjMhnVp6wcM5WX0SYfE130_head.
- NP681606.RAHL6MBiqBGzc0vpUp5KUiRRVOhjMhnVp6wcM5WX0SYfE130_assertion description "[The most common cause of inherited SCA was a mutation at the SCA6 locus (25%), followed by mutation at the SCA1 locus (15%), SCA3 locus (5%) and dentatorubral-pallidoluysian atrophy locus (5%).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP681606.RAHL6MBiqBGzc0vpUp5KUiRRVOhjMhnVp6wcM5WX0SYfE130_provenance.
- NP681606.RAHL6MBiqBGzc0vpUp5KUiRRVOhjMhnVp6wcM5WX0SYfE130_assertion evidence source_evidence_literature NP681606.RAHL6MBiqBGzc0vpUp5KUiRRVOhjMhnVp6wcM5WX0SYfE130_provenance.
- NP681606.RAHL6MBiqBGzc0vpUp5KUiRRVOhjMhnVp6wcM5WX0SYfE130_assertion SIO_000772 11359084 NP681606.RAHL6MBiqBGzc0vpUp5KUiRRVOhjMhnVp6wcM5WX0SYfE130_provenance.
- NP681606.RAHL6MBiqBGzc0vpUp5KUiRRVOhjMhnVp6wcM5WX0SYfE130_assertion wasDerivedFrom befree-20150227 NP681606.RAHL6MBiqBGzc0vpUp5KUiRRVOhjMhnVp6wcM5WX0SYfE130_provenance.
- NP681606.RAHL6MBiqBGzc0vpUp5KUiRRVOhjMhnVp6wcM5WX0SYfE130_assertion wasGeneratedBy ECO_0000203 NP681606.RAHL6MBiqBGzc0vpUp5KUiRRVOhjMhnVp6wcM5WX0SYfE130_provenance.