Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP1260385.RACNjWxYWzqp69kq3Rr4ApbYqSDD44rw3hvUtohCxCI2c130_assertion> ?p ?o ?g. }
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- NP1260385.RACNjWxYWzqp69kq3Rr4ApbYqSDD44rw3hvUtohCxCI2c130_assertion type Assertion NP1260385.RACNjWxYWzqp69kq3Rr4ApbYqSDD44rw3hvUtohCxCI2c130_head.
- 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.
- NP1260385.RACNjWxYWzqp69kq3Rr4ApbYqSDD44rw3hvUtohCxCI2c130_assertion evidence source_evidence_literature NP1260385.RACNjWxYWzqp69kq3Rr4ApbYqSDD44rw3hvUtohCxCI2c130_provenance.
- NP1260385.RACNjWxYWzqp69kq3Rr4ApbYqSDD44rw3hvUtohCxCI2c130_assertion SIO_000772 25644864 NP1260385.RACNjWxYWzqp69kq3Rr4ApbYqSDD44rw3hvUtohCxCI2c130_provenance.
- NP1260385.RACNjWxYWzqp69kq3Rr4ApbYqSDD44rw3hvUtohCxCI2c130_assertion wasDerivedFrom befree-2016 NP1260385.RACNjWxYWzqp69kq3Rr4ApbYqSDD44rw3hvUtohCxCI2c130_provenance.
- NP1260385.RACNjWxYWzqp69kq3Rr4ApbYqSDD44rw3hvUtohCxCI2c130_assertion wasGeneratedBy ECO_0000203 NP1260385.RACNjWxYWzqp69kq3Rr4ApbYqSDD44rw3hvUtohCxCI2c130_provenance.