Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP923797.RAfzQq3gPSf4ikcoZfEmW4d-jnc8Ke2cRXkSwhglcdThs130_assertion> ?p ?o ?g. }
Showing items 1 to 6 of
6
with 100 items per page.
- NP923797.RAfzQq3gPSf4ikcoZfEmW4d-jnc8Ke2cRXkSwhglcdThs130_assertion type Assertion NP923797.RAfzQq3gPSf4ikcoZfEmW4d-jnc8Ke2cRXkSwhglcdThs130_head.
- NP923797.RAfzQq3gPSf4ikcoZfEmW4d-jnc8Ke2cRXkSwhglcdThs130_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." NP923797.RAfzQq3gPSf4ikcoZfEmW4d-jnc8Ke2cRXkSwhglcdThs130_provenance.
- NP923797.RAfzQq3gPSf4ikcoZfEmW4d-jnc8Ke2cRXkSwhglcdThs130_assertion evidence source_evidence_literature NP923797.RAfzQq3gPSf4ikcoZfEmW4d-jnc8Ke2cRXkSwhglcdThs130_provenance.
- NP923797.RAfzQq3gPSf4ikcoZfEmW4d-jnc8Ke2cRXkSwhglcdThs130_assertion SIO_000772 15979648 NP923797.RAfzQq3gPSf4ikcoZfEmW4d-jnc8Ke2cRXkSwhglcdThs130_provenance.
- NP923797.RAfzQq3gPSf4ikcoZfEmW4d-jnc8Ke2cRXkSwhglcdThs130_assertion wasDerivedFrom befree-20150227 NP923797.RAfzQq3gPSf4ikcoZfEmW4d-jnc8Ke2cRXkSwhglcdThs130_provenance.
- NP923797.RAfzQq3gPSf4ikcoZfEmW4d-jnc8Ke2cRXkSwhglcdThs130_assertion wasGeneratedBy ECO_0000203 NP923797.RAfzQq3gPSf4ikcoZfEmW4d-jnc8Ke2cRXkSwhglcdThs130_provenance.