Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP177489.RA2nQZMtQOqebZfOQllHK5-_pJjDK41drwoFGHa3toJ58130_assertion> ?p ?o ?g. }
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- NP177489.RA2nQZMtQOqebZfOQllHK5-_pJjDK41drwoFGHa3toJ58130_assertion type Assertion NP177489.RA2nQZMtQOqebZfOQllHK5-_pJjDK41drwoFGHa3toJ58130_head.
- NP177489.RA2nQZMtQOqebZfOQllHK5-_pJjDK41drwoFGHa3toJ58130_assertion description "[Friedreich's ataxia (FRDA) is an autosomal recessive disease caused by mutations that produce a deficiency in frataxin.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP177489.RA2nQZMtQOqebZfOQllHK5-_pJjDK41drwoFGHa3toJ58130_provenance.
- NP177489.RA2nQZMtQOqebZfOQllHK5-_pJjDK41drwoFGHa3toJ58130_assertion evidence source_evidence_literature NP177489.RA2nQZMtQOqebZfOQllHK5-_pJjDK41drwoFGHa3toJ58130_provenance.
- NP177489.RA2nQZMtQOqebZfOQllHK5-_pJjDK41drwoFGHa3toJ58130_assertion SIO_000772 21531789 NP177489.RA2nQZMtQOqebZfOQllHK5-_pJjDK41drwoFGHa3toJ58130_provenance.
- NP177489.RA2nQZMtQOqebZfOQllHK5-_pJjDK41drwoFGHa3toJ58130_assertion wasDerivedFrom befree-20140225 NP177489.RA2nQZMtQOqebZfOQllHK5-_pJjDK41drwoFGHa3toJ58130_provenance.
- NP177489.RA2nQZMtQOqebZfOQllHK5-_pJjDK41drwoFGHa3toJ58130_assertion wasGeneratedBy ECO_0000203 NP177489.RA2nQZMtQOqebZfOQllHK5-_pJjDK41drwoFGHa3toJ58130_provenance.