Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP411517.RAJVh3Fs5zB4ajTdhJ9AKmpH5DRc0FdBQuipy0yu1n9rE130_assertion> ?p ?o ?g. }
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- NP411517.RAJVh3Fs5zB4ajTdhJ9AKmpH5DRc0FdBQuipy0yu1n9rE130_assertion type Assertion NP411517.RAJVh3Fs5zB4ajTdhJ9AKmpH5DRc0FdBQuipy0yu1n9rE130_head.
- NP411517.RAJVh3Fs5zB4ajTdhJ9AKmpH5DRc0FdBQuipy0yu1n9rE130_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." NP411517.RAJVh3Fs5zB4ajTdhJ9AKmpH5DRc0FdBQuipy0yu1n9rE130_provenance.
- NP411517.RAJVh3Fs5zB4ajTdhJ9AKmpH5DRc0FdBQuipy0yu1n9rE130_assertion evidence source_evidence_literature NP411517.RAJVh3Fs5zB4ajTdhJ9AKmpH5DRc0FdBQuipy0yu1n9rE130_provenance.
- NP411517.RAJVh3Fs5zB4ajTdhJ9AKmpH5DRc0FdBQuipy0yu1n9rE130_assertion SIO_000772 9463307 NP411517.RAJVh3Fs5zB4ajTdhJ9AKmpH5DRc0FdBQuipy0yu1n9rE130_provenance.
- NP411517.RAJVh3Fs5zB4ajTdhJ9AKmpH5DRc0FdBQuipy0yu1n9rE130_assertion wasDerivedFrom befree-20150227 NP411517.RAJVh3Fs5zB4ajTdhJ9AKmpH5DRc0FdBQuipy0yu1n9rE130_provenance.
- NP411517.RAJVh3Fs5zB4ajTdhJ9AKmpH5DRc0FdBQuipy0yu1n9rE130_assertion wasGeneratedBy ECO_0000203 NP411517.RAJVh3Fs5zB4ajTdhJ9AKmpH5DRc0FdBQuipy0yu1n9rE130_provenance.