Matches in Nanopublications for { ?s ?p "[Asp58Ala is the predominant mutation of the TTR gene in Korean patients with hereditary transthyretin-related amyloidosis.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ?g. }
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- assertion description "[Asp58Ala is the predominant mutation of the TTR gene in Korean patients with hereditary transthyretin-related amyloidosis.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
- NP1260385.RACNjWxYWzqp69kq3Rr4ApbYqSDD44rw3hvUtohCxCI2c130_assertion description "[Asp58Ala is the predominant mutation of the TTR gene in Korean patients with hereditary transthyretin-related amyloidosis.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1260385.RACNjWxYWzqp69kq3Rr4ApbYqSDD44rw3hvUtohCxCI2c130_provenance.