Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP276976.RAI8m2L-YJFXrkzn45z4CbS3goQahXgB35B4VoOJswIsw130_assertion> ?p ?o ?g. }
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- NP276976.RAI8m2L-YJFXrkzn45z4CbS3goQahXgB35B4VoOJswIsw130_assertion type Assertion NP276976.RAI8m2L-YJFXrkzn45z4CbS3goQahXgB35B4VoOJswIsw130_head.
- NP276976.RAI8m2L-YJFXrkzn45z4CbS3goQahXgB35B4VoOJswIsw130_assertion description "[We found that SCA3/MJD was the most common type of autosomal dominant SCA in Mainland Chinese, accounting for 83 patients from 59 families (49.2%), followed by SCA2 (8 [6.7%]), SCA1 (7 [5.8%]), SCA6 (4 [3.3%]), SCA7 (1 [0.8%]), SCA8 (0%), SCA10 (0%), SCA12 (1 [0.8%]), SCA14 (0%), SCA17 (0%) and DRPLA (0%).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP276976.RAI8m2L-YJFXrkzn45z4CbS3goQahXgB35B4VoOJswIsw130_provenance.
- NP276976.RAI8m2L-YJFXrkzn45z4CbS3goQahXgB35B4VoOJswIsw130_assertion evidence source_evidence_literature NP276976.RAI8m2L-YJFXrkzn45z4CbS3goQahXgB35B4VoOJswIsw130_provenance.
- NP276976.RAI8m2L-YJFXrkzn45z4CbS3goQahXgB35B4VoOJswIsw130_assertion SIO_000772 15979648 NP276976.RAI8m2L-YJFXrkzn45z4CbS3goQahXgB35B4VoOJswIsw130_provenance.
- NP276976.RAI8m2L-YJFXrkzn45z4CbS3goQahXgB35B4VoOJswIsw130_assertion wasDerivedFrom befree-20150227 NP276976.RAI8m2L-YJFXrkzn45z4CbS3goQahXgB35B4VoOJswIsw130_provenance.
- NP276976.RAI8m2L-YJFXrkzn45z4CbS3goQahXgB35B4VoOJswIsw130_assertion wasGeneratedBy ECO_0000203 NP276976.RAI8m2L-YJFXrkzn45z4CbS3goQahXgB35B4VoOJswIsw130_provenance.