Matches in Nanopublications for { ?s ?p "[PMM2-CDG (formerly known as CDG Ia) a deficiency in phosphomannomutase, is the most frequent congenital disorder of glycosylation.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ?g. }
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- assertion description "[PMM2-CDG (formerly known as CDG Ia) a deficiency in phosphomannomutase, is the most frequent congenital disorder of glycosylation.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
- NP1246998.RAXNZfBYSTSwycnAKFZEW5gizLXOu6Ky1b4tJNMcA5YvU130_assertion description "[PMM2-CDG (formerly known as CDG Ia) a deficiency in phosphomannomutase, is the most frequent congenital disorder of glycosylation.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1246998.RAXNZfBYSTSwycnAKFZEW5gizLXOu6Ky1b4tJNMcA5YvU130_provenance.