Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP256409.RAIyrjX-shgABhc9W507dCyx0CT3oD-j4Qg8HTx6lUVJE130_assertion> ?p ?o ?g. }
Showing items 1 to 6 of
6
with 100 items per page.
- NP256409.RAIyrjX-shgABhc9W507dCyx0CT3oD-j4Qg8HTx6lUVJE130_assertion type Assertion NP256409.RAIyrjX-shgABhc9W507dCyx0CT3oD-j4Qg8HTx6lUVJE130_head.
- NP256409.RAIyrjX-shgABhc9W507dCyx0CT3oD-j4Qg8HTx6lUVJE130_assertion description "[Clinical and genetic analysis of three German kindreds with autosomal dominant cerebellar ataxia type I linked to the SCA2 locus.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP256409.RAIyrjX-shgABhc9W507dCyx0CT3oD-j4Qg8HTx6lUVJE130_provenance.
- NP256409.RAIyrjX-shgABhc9W507dCyx0CT3oD-j4Qg8HTx6lUVJE130_assertion evidence source_evidence_literature NP256409.RAIyrjX-shgABhc9W507dCyx0CT3oD-j4Qg8HTx6lUVJE130_provenance.
- NP256409.RAIyrjX-shgABhc9W507dCyx0CT3oD-j4Qg8HTx6lUVJE130_assertion SIO_000772 9112595 NP256409.RAIyrjX-shgABhc9W507dCyx0CT3oD-j4Qg8HTx6lUVJE130_provenance.
- NP256409.RAIyrjX-shgABhc9W507dCyx0CT3oD-j4Qg8HTx6lUVJE130_assertion wasDerivedFrom befree-20140225 NP256409.RAIyrjX-shgABhc9W507dCyx0CT3oD-j4Qg8HTx6lUVJE130_provenance.
- NP256409.RAIyrjX-shgABhc9W507dCyx0CT3oD-j4Qg8HTx6lUVJE130_assertion wasGeneratedBy ECO_0000203 NP256409.RAIyrjX-shgABhc9W507dCyx0CT3oD-j4Qg8HTx6lUVJE130_provenance.