Matches in Nanopublications for { ?s ?p "[The apparent mineralocorticoid excess syndrome (AME) is a rare autosomal recessive disorder due to the deficiency of 11beta-hydroxysteroid dehydrogenase type 2 enzyme (11beta-HSD2).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ?g. }
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- NP285544.RAUASSfBljzthsOoZde60oiajgc5jXvD5fpj6JMjjSG4s130_assertion description "[The apparent mineralocorticoid excess syndrome (AME) is a rare autosomal recessive disorder due to the deficiency of 11beta-hydroxysteroid dehydrogenase type 2 enzyme (11beta-HSD2).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP285544.RAUASSfBljzthsOoZde60oiajgc5jXvD5fpj6JMjjSG4s130_provenance.
- NP154869.RAmPCVarnoUQ5LKxrCyN8R_w_oZW-n9CyKSh6wPWwwa1M130_assertion description "[The apparent mineralocorticoid excess syndrome (AME) is a rare autosomal recessive disorder due to the deficiency of 11beta-hydroxysteroid dehydrogenase type 2 enzyme (11beta-HSD2).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP154869.RAmPCVarnoUQ5LKxrCyN8R_w_oZW-n9CyKSh6wPWwwa1M130_provenance.