Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP225872.RAdsCnDGaYEMKLoOm208VMsFI1uQMtbCXDW8uG_0Tdyv8130_assertion> ?p ?o ?g. }
Showing items 1 to 6 of
6
with 100 items per page.
- NP225872.RAdsCnDGaYEMKLoOm208VMsFI1uQMtbCXDW8uG_0Tdyv8130_assertion type Assertion NP225872.RAdsCnDGaYEMKLoOm208VMsFI1uQMtbCXDW8uG_0Tdyv8130_head.
- NP225872.RAdsCnDGaYEMKLoOm208VMsFI1uQMtbCXDW8uG_0Tdyv8130_assertion description "[Spinocerebellar ataxia type 6 (SCA6) was recently identified as a form of autosomal dominant spinocerebellar ataxia associated with a small CAG repeat expansion of the gene encoding an alpha 1 A-voltage-dependent calcium channel gene subunit on chromosome 19p13.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP225872.RAdsCnDGaYEMKLoOm208VMsFI1uQMtbCXDW8uG_0Tdyv8130_provenance.
- NP225872.RAdsCnDGaYEMKLoOm208VMsFI1uQMtbCXDW8uG_0Tdyv8130_assertion evidence source_evidence_literature NP225872.RAdsCnDGaYEMKLoOm208VMsFI1uQMtbCXDW8uG_0Tdyv8130_provenance.
- NP225872.RAdsCnDGaYEMKLoOm208VMsFI1uQMtbCXDW8uG_0Tdyv8130_assertion SIO_000772 10985694 NP225872.RAdsCnDGaYEMKLoOm208VMsFI1uQMtbCXDW8uG_0Tdyv8130_provenance.
- NP225872.RAdsCnDGaYEMKLoOm208VMsFI1uQMtbCXDW8uG_0Tdyv8130_assertion wasDerivedFrom befree-20150227 NP225872.RAdsCnDGaYEMKLoOm208VMsFI1uQMtbCXDW8uG_0Tdyv8130_provenance.
- NP225872.RAdsCnDGaYEMKLoOm208VMsFI1uQMtbCXDW8uG_0Tdyv8130_assertion wasGeneratedBy ECO_0000203 NP225872.RAdsCnDGaYEMKLoOm208VMsFI1uQMtbCXDW8uG_0Tdyv8130_provenance.