Matches in Nanopublications for { ?s ?p "[Human acute intermittent porphyria (AIP), the most common acute hepatic porphyria, is an autosomal dominant inborn error of heme biosynthesis due to the half-normal activity of hydroxymethylbilane synthase (HMB-synthase).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ?g. }
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- NP921376.RADsQYBwa8BS6ZGL450pIFC0pdgkAprh6-V3uNsPbTkdY130_assertion description "[Human acute intermittent porphyria (AIP), the most common acute hepatic porphyria, is an autosomal dominant inborn error of heme biosynthesis due to the half-normal activity of hydroxymethylbilane synthase (HMB-synthase).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP921376.RADsQYBwa8BS6ZGL450pIFC0pdgkAprh6-V3uNsPbTkdY130_provenance.
- NP459231.RAak_5_KuJcA6Guv7cauVUhXe-418Kszdn02YuKQwKFoY130_assertion description "[Human acute intermittent porphyria (AIP), the most common acute hepatic porphyria, is an autosomal dominant inborn error of heme biosynthesis due to the half-normal activity of hydroxymethylbilane synthase (HMB-synthase).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP459231.RAak_5_KuJcA6Guv7cauVUhXe-418Kszdn02YuKQwKFoY130_provenance.
- NP777409.RA4N-hmBDVpQ7nhJ9J2rEjc4eMcghJggy5naxh4sEydCg130_assertion description "[Human acute intermittent porphyria (AIP), the most common acute hepatic porphyria, is an autosomal dominant inborn error of heme biosynthesis due to the half-normal activity of hydroxymethylbilane synthase (HMB-synthase).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP777409.RA4N-hmBDVpQ7nhJ9J2rEjc4eMcghJggy5naxh4sEydCg130_provenance.