Matches in Nanopublications for { ?s ?p "[Persistent trimethylaminuria in children is caused by autosomal recessively inherited impairment of hepatic trimethylamine (TMA) oxidation due to deficiency of flavin monooxygenase 3 (FMO3) secondary to mutations in the FMO3 gene.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ?g. }
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- NP310025.RAjM6C0X4yix6Odmam4QbpERhTHwZa7QF5heMOnE3d79k130_assertion description "[Persistent trimethylaminuria in children is caused by autosomal recessively inherited impairment of hepatic trimethylamine (TMA) oxidation due to deficiency of flavin monooxygenase 3 (FMO3) secondary to mutations in the FMO3 gene.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP310025.RAjM6C0X4yix6Odmam4QbpERhTHwZa7QF5heMOnE3d79k130_provenance.
- assertion description "[Persistent trimethylaminuria in children is caused by autosomal recessively inherited impairment of hepatic trimethylamine (TMA) oxidation due to deficiency of flavin monooxygenase 3 (FMO3) secondary to mutations in the FMO3 gene.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.