Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP472613.RA1h788BK9BUkj34jQDd0LWJScsLxmEdWuynmKYOopMRA130_assertion> ?p ?o ?g. }
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- NP472613.RA1h788BK9BUkj34jQDd0LWJScsLxmEdWuynmKYOopMRA130_assertion type Assertion NP472613.RA1h788BK9BUkj34jQDd0LWJScsLxmEdWuynmKYOopMRA130_head.
- NP472613.RA1h788BK9BUkj34jQDd0LWJScsLxmEdWuynmKYOopMRA130_assertion description "[Three patients with AOA1 were identified in an APTX mutation screening on 28 Southern Italian patients with progressive ataxia and peripheral neuropathy.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP472613.RA1h788BK9BUkj34jQDd0LWJScsLxmEdWuynmKYOopMRA130_provenance.
- NP472613.RA1h788BK9BUkj34jQDd0LWJScsLxmEdWuynmKYOopMRA130_assertion evidence source_evidence_literature NP472613.RA1h788BK9BUkj34jQDd0LWJScsLxmEdWuynmKYOopMRA130_provenance.
- NP472613.RA1h788BK9BUkj34jQDd0LWJScsLxmEdWuynmKYOopMRA130_assertion SIO_000772 15596775 NP472613.RA1h788BK9BUkj34jQDd0LWJScsLxmEdWuynmKYOopMRA130_provenance.
- NP472613.RA1h788BK9BUkj34jQDd0LWJScsLxmEdWuynmKYOopMRA130_assertion wasDerivedFrom befree-2016 NP472613.RA1h788BK9BUkj34jQDd0LWJScsLxmEdWuynmKYOopMRA130_provenance.
- NP472613.RA1h788BK9BUkj34jQDd0LWJScsLxmEdWuynmKYOopMRA130_assertion wasGeneratedBy ECO_0000203 NP472613.RA1h788BK9BUkj34jQDd0LWJScsLxmEdWuynmKYOopMRA130_provenance.