Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP914759.RAsDu0TLiM9IP3Mg8p3F0trUacn3sI_DdyOUolsvEQhGM130_assertion> ?p ?o ?g. }
Showing items 1 to 6 of
6
with 100 items per page.
- NP914759.RAsDu0TLiM9IP3Mg8p3F0trUacn3sI_DdyOUolsvEQhGM130_assertion type Assertion NP914759.RAsDu0TLiM9IP3Mg8p3F0trUacn3sI_DdyOUolsvEQhGM130_head.
- NP914759.RAsDu0TLiM9IP3Mg8p3F0trUacn3sI_DdyOUolsvEQhGM130_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." NP914759.RAsDu0TLiM9IP3Mg8p3F0trUacn3sI_DdyOUolsvEQhGM130_provenance.
- NP914759.RAsDu0TLiM9IP3Mg8p3F0trUacn3sI_DdyOUolsvEQhGM130_assertion evidence source_evidence_literature NP914759.RAsDu0TLiM9IP3Mg8p3F0trUacn3sI_DdyOUolsvEQhGM130_provenance.
- NP914759.RAsDu0TLiM9IP3Mg8p3F0trUacn3sI_DdyOUolsvEQhGM130_assertion SIO_000772 15596775 NP914759.RAsDu0TLiM9IP3Mg8p3F0trUacn3sI_DdyOUolsvEQhGM130_provenance.
- NP914759.RAsDu0TLiM9IP3Mg8p3F0trUacn3sI_DdyOUolsvEQhGM130_assertion wasDerivedFrom befree-20150227 NP914759.RAsDu0TLiM9IP3Mg8p3F0trUacn3sI_DdyOUolsvEQhGM130_provenance.
- NP914759.RAsDu0TLiM9IP3Mg8p3F0trUacn3sI_DdyOUolsvEQhGM130_assertion wasGeneratedBy ECO_0000203 NP914759.RAsDu0TLiM9IP3Mg8p3F0trUacn3sI_DdyOUolsvEQhGM130_provenance.