Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP1388572.RApLEYZ8HRTOAuLHLswjXVHnk4elxY2AtfFa2mK_XVXas130_assertion> ?p ?o ?g. }
Showing items 1 to 6 of
6
with 100 items per page.
- NP1388572.RApLEYZ8HRTOAuLHLswjXVHnk4elxY2AtfFa2mK_XVXas130_assertion type Assertion NP1388572.RApLEYZ8HRTOAuLHLswjXVHnk4elxY2AtfFa2mK_XVXas130_head.
- NP1388572.RApLEYZ8HRTOAuLHLswjXVHnk4elxY2AtfFa2mK_XVXas130_assertion description "[Ataxia with vitamin E deficiency (AVED), or familial isolated vitamin E deficiency, is a rare autosomal recessive neurodegenerative disease characterized clinically by symptoms with often striking resemblance to those of Friedreich ataxia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1388572.RApLEYZ8HRTOAuLHLswjXVHnk4elxY2AtfFa2mK_XVXas130_provenance.
- NP1388572.RApLEYZ8HRTOAuLHLswjXVHnk4elxY2AtfFa2mK_XVXas130_assertion evidence source_evidence_literature NP1388572.RApLEYZ8HRTOAuLHLswjXVHnk4elxY2AtfFa2mK_XVXas130_provenance.
- NP1388572.RApLEYZ8HRTOAuLHLswjXVHnk4elxY2AtfFa2mK_XVXas130_assertion SIO_000772 9463307 NP1388572.RApLEYZ8HRTOAuLHLswjXVHnk4elxY2AtfFa2mK_XVXas130_provenance.
- NP1388572.RApLEYZ8HRTOAuLHLswjXVHnk4elxY2AtfFa2mK_XVXas130_assertion wasDerivedFrom befree-2016 NP1388572.RApLEYZ8HRTOAuLHLswjXVHnk4elxY2AtfFa2mK_XVXas130_provenance.
- NP1388572.RApLEYZ8HRTOAuLHLswjXVHnk4elxY2AtfFa2mK_XVXas130_assertion wasGeneratedBy ECO_0000203 NP1388572.RApLEYZ8HRTOAuLHLswjXVHnk4elxY2AtfFa2mK_XVXas130_provenance.