Matches in Nanopublications for { ?s ?p "[Catalytic deficiency of human aldolase B in hereditary fructose intolerance caused by a common missense mutation.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ?g. }
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- assertion description "[Catalytic deficiency of human aldolase B in hereditary fructose intolerance caused by a common missense mutation.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
- NP8439.RA_efF_kbdnJfTgCp1x5rXQi0U_sX2FlStFa8Pi3LxgsM130_assertion description "[Catalytic deficiency of human aldolase B in hereditary fructose intolerance caused by a common missense mutation.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP8439.RA_efF_kbdnJfTgCp1x5rXQi0U_sX2FlStFa8Pi3LxgsM130_provenance.
- NP36033.RAbGmPrc2cYihmSZU3KFQLwe6zX5TXgOYmfElb0SNNZq4130_assertion description "[Catalytic deficiency of human aldolase B in hereditary fructose intolerance caused by a common missense mutation.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP36033.RAbGmPrc2cYihmSZU3KFQLwe6zX5TXgOYmfElb0SNNZq4130_provenance.
- NP6689.RALvCpexguxeLySf85X5YXon5JcEyIW0_fub3yTM-9kU8130_assertion description "[Catalytic deficiency of human aldolase B in hereditary fructose intolerance caused by a common missense mutation.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP6689.RALvCpexguxeLySf85X5YXon5JcEyIW0_fub3yTM-9kU8130_provenance.