Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP1326607.RA5t5mHbcJUthSU3UGYAE1ChohMC41uq7buEQ2_lKkGA8#assertion> ?p ?o ?g. }
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- 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." provenance.
- assertion evidence source_evidence_literature provenance.
- assertion SIO_000772 15596775 provenance.
- assertion wasDerivedFrom BEFREE provenance.
- assertion wasGeneratedBy ECO_0000203 provenance.