Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP197728.RAqrNjUI4tPmiUCFOineaN6OMveOUDouRbqMyTV4nuhkU130_assertion> ?p ?o ?g. }
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- NP197728.RAqrNjUI4tPmiUCFOineaN6OMveOUDouRbqMyTV4nuhkU130_assertion type Assertion NP197728.RAqrNjUI4tPmiUCFOineaN6OMveOUDouRbqMyTV4nuhkU130_head.
- NP197728.RAqrNjUI4tPmiUCFOineaN6OMveOUDouRbqMyTV4nuhkU130_assertion description "[Among the 16 families with an apparently recessive mode of ataxia inheritance, 4 (25%) were identified as having the FRDA mutation.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP197728.RAqrNjUI4tPmiUCFOineaN6OMveOUDouRbqMyTV4nuhkU130_provenance.
- NP197728.RAqrNjUI4tPmiUCFOineaN6OMveOUDouRbqMyTV4nuhkU130_assertion evidence source_evidence_literature NP197728.RAqrNjUI4tPmiUCFOineaN6OMveOUDouRbqMyTV4nuhkU130_provenance.
- NP197728.RAqrNjUI4tPmiUCFOineaN6OMveOUDouRbqMyTV4nuhkU130_assertion SIO_000772 16149098 NP197728.RAqrNjUI4tPmiUCFOineaN6OMveOUDouRbqMyTV4nuhkU130_provenance.
- NP197728.RAqrNjUI4tPmiUCFOineaN6OMveOUDouRbqMyTV4nuhkU130_assertion wasDerivedFrom befree-20140225 NP197728.RAqrNjUI4tPmiUCFOineaN6OMveOUDouRbqMyTV4nuhkU130_provenance.
- NP197728.RAqrNjUI4tPmiUCFOineaN6OMveOUDouRbqMyTV4nuhkU130_assertion wasGeneratedBy ECO_0000203 NP197728.RAqrNjUI4tPmiUCFOineaN6OMveOUDouRbqMyTV4nuhkU130_provenance.