Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP387352.RAqkhj9p1NogVK474KVEsUJTP1xk_w9o17vY71ryKig8g130_assertion> ?p ?o ?g. }
Showing items 1 to 6 of
6
with 100 items per page.
- NP387352.RAqkhj9p1NogVK474KVEsUJTP1xk_w9o17vY71ryKig8g130_assertion type Assertion NP387352.RAqkhj9p1NogVK474KVEsUJTP1xk_w9o17vY71ryKig8g130_head.
- NP387352.RAqkhj9p1NogVK474KVEsUJTP1xk_w9o17vY71ryKig8g130_assertion wasGeneratedBy ECO_0000203 NP387352.RAqkhj9p1NogVK474KVEsUJTP1xk_w9o17vY71ryKig8g130_provenance.
- NP387352.RAqkhj9p1NogVK474KVEsUJTP1xk_w9o17vY71ryKig8g130_assertion wasDerivedFrom befree-20140225 NP387352.RAqkhj9p1NogVK474KVEsUJTP1xk_w9o17vY71ryKig8g130_provenance.
- NP387352.RAqkhj9p1NogVK474KVEsUJTP1xk_w9o17vY71ryKig8g130_assertion SIO_000772 10399872 NP387352.RAqkhj9p1NogVK474KVEsUJTP1xk_w9o17vY71ryKig8g130_provenance.
- NP387352.RAqkhj9p1NogVK474KVEsUJTP1xk_w9o17vY71ryKig8g130_assertion evidence source_evidence_literature NP387352.RAqkhj9p1NogVK474KVEsUJTP1xk_w9o17vY71ryKig8g130_provenance.
- NP387352.RAqkhj9p1NogVK474KVEsUJTP1xk_w9o17vY71ryKig8g130_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." NP387352.RAqkhj9p1NogVK474KVEsUJTP1xk_w9o17vY71ryKig8g130_provenance.