Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP6415.RAhO5YbMAWEECy0o5CWrBx9xhpPgM7FsKEHjezjHkE8pQ130_assertion> ?p ?o ?g. }
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- NP6415.RAhO5YbMAWEECy0o5CWrBx9xhpPgM7FsKEHjezjHkE8pQ130_assertion type Assertion NP6415.RAhO5YbMAWEECy0o5CWrBx9xhpPgM7FsKEHjezjHkE8pQ130_head.
- NP6415.RAhO5YbMAWEECy0o5CWrBx9xhpPgM7FsKEHjezjHkE8pQ130_assertion wasGeneratedBy ECO_0000218 NP6415.RAhO5YbMAWEECy0o5CWrBx9xhpPgM7FsKEHjezjHkE8pQ130_provenance.
- NP6415.RAhO5YbMAWEECy0o5CWrBx9xhpPgM7FsKEHjezjHkE8pQ130_assertion wasDerivedFrom uniprot-2016 NP6415.RAhO5YbMAWEECy0o5CWrBx9xhpPgM7FsKEHjezjHkE8pQ130_provenance.
- NP6415.RAhO5YbMAWEECy0o5CWrBx9xhpPgM7FsKEHjezjHkE8pQ130_assertion SIO_000772 21035104 NP6415.RAhO5YbMAWEECy0o5CWrBx9xhpPgM7FsKEHjezjHkE8pQ130_provenance.
- NP6415.RAhO5YbMAWEECy0o5CWrBx9xhpPgM7FsKEHjezjHkE8pQ130_assertion evidence source_evidence_curated NP6415.RAhO5YbMAWEECy0o5CWrBx9xhpPgM7FsKEHjezjHkE8pQ130_provenance.
- NP6415.RAhO5YbMAWEECy0o5CWrBx9xhpPgM7FsKEHjezjHkE8pQ130_assertion description "[PDYN mutations are identified in a small subset of ataxia families, indicating that SCA23 is an infrequent SCA type (∼0.5%) in the Netherlands and suggesting further genetic SCA heterogeneity.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP6415.RAhO5YbMAWEECy0o5CWrBx9xhpPgM7FsKEHjezjHkE8pQ130_provenance.