Matches in Nanopublications for { ?s ?p "[Mutations generating inactive enzymes have been described in the HSD11B2 gene in the congenital syndrome of apparent mineralocorticoid excess (AME)--a low renin form of hypertension.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ?g. }
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- NP669969.RAa50StxAIIIloveEYi1gXFVGnw4AWKGkxoEH4bnyWdi8130_assertion description "[Mutations generating inactive enzymes have been described in the HSD11B2 gene in the congenital syndrome of apparent mineralocorticoid excess (AME)--a low renin form of hypertension.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP669969.RAa50StxAIIIloveEYi1gXFVGnw4AWKGkxoEH4bnyWdi8130_provenance.
- NP501379.RAExx4Tx3oymoT_okScn0yN6KnJOoVpmT9weOYKSPD9ac130_assertion description "[Mutations generating inactive enzymes have been described in the HSD11B2 gene in the congenital syndrome of apparent mineralocorticoid excess (AME)--a low renin form of hypertension.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP501379.RAExx4Tx3oymoT_okScn0yN6KnJOoVpmT9weOYKSPD9ac130_provenance.
- assertion description "[Mutations generating inactive enzymes have been described in the HSD11B2 gene in the congenital syndrome of apparent mineralocorticoid excess (AME)--a low renin form of hypertension.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
- assertion description "[Mutations generating inactive enzymes have been described in the HSD11B2 gene in the congenital syndrome of apparent mineralocorticoid excess (AME)--a low renin form of hypertension.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
- assertion description "[Mutations generating inactive enzymes have been described in the HSD11B2 gene in the congenital syndrome of apparent mineralocorticoid excess (AME)--a low renin form of hypertension.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
- NP1378029.RAfZpRzW4p0hJkOa9jOtQgB9E92kkIYWwDOHe1uSOFcGc130_assertion description "[Mutations generating inactive enzymes have been described in the HSD11B2 gene in the congenital syndrome of apparent mineralocorticoid excess (AME)--a low renin form of hypertension.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1378029.RAfZpRzW4p0hJkOa9jOtQgB9E92kkIYWwDOHe1uSOFcGc130_provenance.
- NP1378030.RAg2GglBNJjDnk0OcVofWwLqGYln2QIUu6xjimulbwCoM130_assertion description "[Mutations generating inactive enzymes have been described in the HSD11B2 gene in the congenital syndrome of apparent mineralocorticoid excess (AME)--a low renin form of hypertension.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1378030.RAg2GglBNJjDnk0OcVofWwLqGYln2QIUu6xjimulbwCoM130_provenance.
- NP466061.RA4b4zWgADzYU8fd8qCIoOM30aaTTqTAdd4VAuR-ENBlk130_assertion description "[Mutations generating inactive enzymes have been described in the HSD11B2 gene in the congenital syndrome of apparent mineralocorticoid excess (AME)--a low renin form of hypertension.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP466061.RA4b4zWgADzYU8fd8qCIoOM30aaTTqTAdd4VAuR-ENBlk130_provenance.
- NP1378028.RA0mL1ngQ9qcsZjnDlQRiGcSYCviwRumbAPG7H7aDeS08130_assertion description "[Mutations generating inactive enzymes have been described in the HSD11B2 gene in the congenital syndrome of apparent mineralocorticoid excess (AME)--a low renin form of hypertension.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1378028.RA0mL1ngQ9qcsZjnDlQRiGcSYCviwRumbAPG7H7aDeS08130_provenance.