Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP472615.RA7oNMU0CrIVMW8IdwUEhB4zrtvlfi0aj-4LMbs2fd6gQ130_assertion> ?p ?o ?g. }
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- NP472615.RA7oNMU0CrIVMW8IdwUEhB4zrtvlfi0aj-4LMbs2fd6gQ130_assertion type Assertion NP472615.RA7oNMU0CrIVMW8IdwUEhB4zrtvlfi0aj-4LMbs2fd6gQ130_head.
- NP472615.RA7oNMU0CrIVMW8IdwUEhB4zrtvlfi0aj-4LMbs2fd6gQ130_assertion description "[Ataxia with oculomotor apraxia type 1 (AOA1) is an autosomal recessive disorder characterized by early-onset cerebellar ataxia, oculomotor apraxia, and peripheral neuropathy.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP472615.RA7oNMU0CrIVMW8IdwUEhB4zrtvlfi0aj-4LMbs2fd6gQ130_provenance.
- NP472615.RA7oNMU0CrIVMW8IdwUEhB4zrtvlfi0aj-4LMbs2fd6gQ130_assertion evidence source_evidence_literature NP472615.RA7oNMU0CrIVMW8IdwUEhB4zrtvlfi0aj-4LMbs2fd6gQ130_provenance.
- NP472615.RA7oNMU0CrIVMW8IdwUEhB4zrtvlfi0aj-4LMbs2fd6gQ130_assertion SIO_000772 15596775 NP472615.RA7oNMU0CrIVMW8IdwUEhB4zrtvlfi0aj-4LMbs2fd6gQ130_provenance.
- NP472615.RA7oNMU0CrIVMW8IdwUEhB4zrtvlfi0aj-4LMbs2fd6gQ130_assertion wasDerivedFrom befree-2016 NP472615.RA7oNMU0CrIVMW8IdwUEhB4zrtvlfi0aj-4LMbs2fd6gQ130_provenance.
- NP472615.RA7oNMU0CrIVMW8IdwUEhB4zrtvlfi0aj-4LMbs2fd6gQ130_assertion wasGeneratedBy ECO_0000203 NP472615.RA7oNMU0CrIVMW8IdwUEhB4zrtvlfi0aj-4LMbs2fd6gQ130_provenance.