Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP580634.RA7spHilyIAyxjkt_sntKryZ2jMkxVVRhuKz6i-AcJPuE130_assertion> ?p ?o ?g. }
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- NP580634.RA7spHilyIAyxjkt_sntKryZ2jMkxVVRhuKz6i-AcJPuE130_assertion type Assertion NP580634.RA7spHilyIAyxjkt_sntKryZ2jMkxVVRhuKz6i-AcJPuE130_head.
- NP580634.RA7spHilyIAyxjkt_sntKryZ2jMkxVVRhuKz6i-AcJPuE130_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." NP580634.RA7spHilyIAyxjkt_sntKryZ2jMkxVVRhuKz6i-AcJPuE130_provenance.
- NP580634.RA7spHilyIAyxjkt_sntKryZ2jMkxVVRhuKz6i-AcJPuE130_assertion evidence source_evidence_literature NP580634.RA7spHilyIAyxjkt_sntKryZ2jMkxVVRhuKz6i-AcJPuE130_provenance.
- NP580634.RA7spHilyIAyxjkt_sntKryZ2jMkxVVRhuKz6i-AcJPuE130_assertion SIO_000772 9463307 NP580634.RA7spHilyIAyxjkt_sntKryZ2jMkxVVRhuKz6i-AcJPuE130_provenance.
- NP580634.RA7spHilyIAyxjkt_sntKryZ2jMkxVVRhuKz6i-AcJPuE130_assertion wasDerivedFrom befree-20140225 NP580634.RA7spHilyIAyxjkt_sntKryZ2jMkxVVRhuKz6i-AcJPuE130_provenance.
- NP580634.RA7spHilyIAyxjkt_sntKryZ2jMkxVVRhuKz6i-AcJPuE130_assertion wasGeneratedBy ECO_0000203 NP580634.RA7spHilyIAyxjkt_sntKryZ2jMkxVVRhuKz6i-AcJPuE130_provenance.