Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP381890.RArqzsAMXdh856RJipUiK9GHfKeX98m50LVX5NXgx1Kq8130_assertion> ?p ?o ?g. }
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- NP381890.RArqzsAMXdh856RJipUiK9GHfKeX98m50LVX5NXgx1Kq8130_assertion type Assertion NP381890.RArqzsAMXdh856RJipUiK9GHfKeX98m50LVX5NXgx1Kq8130_head.
- NP381890.RArqzsAMXdh856RJipUiK9GHfKeX98m50LVX5NXgx1Kq8130_assertion description "[We clinically and genetically evaluated 73 Italian families with autosomal dominant cerebellar ataxia (ADCA) type I. Spinocerebellar ataxia (SCA) type 1 was the most common genotype (SCA1), accounting for 41% of cases (30 families), SCA2 was slightly less frequent (29%, 21 families), and the remaining families were negative for the SCA1, SCA2, and SCA3 mutations.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP381890.RArqzsAMXdh856RJipUiK9GHfKeX98m50LVX5NXgx1Kq8130_provenance.
- NP381890.RArqzsAMXdh856RJipUiK9GHfKeX98m50LVX5NXgx1Kq8130_assertion evidence source_evidence_literature NP381890.RArqzsAMXdh856RJipUiK9GHfKeX98m50LVX5NXgx1Kq8130_provenance.
- NP381890.RArqzsAMXdh856RJipUiK9GHfKeX98m50LVX5NXgx1Kq8130_assertion SIO_000772 10399872 NP381890.RArqzsAMXdh856RJipUiK9GHfKeX98m50LVX5NXgx1Kq8130_provenance.
- NP381890.RArqzsAMXdh856RJipUiK9GHfKeX98m50LVX5NXgx1Kq8130_assertion wasDerivedFrom befree-20140225 NP381890.RArqzsAMXdh856RJipUiK9GHfKeX98m50LVX5NXgx1Kq8130_provenance.
- NP381890.RArqzsAMXdh856RJipUiK9GHfKeX98m50LVX5NXgx1Kq8130_assertion wasGeneratedBy ECO_0000203 NP381890.RArqzsAMXdh856RJipUiK9GHfKeX98m50LVX5NXgx1Kq8130_provenance.