Matches in Nanopublications for { ?s ?p "[Familial central diabetes insipidus is an inherited disease of predominant autosomal dominant trait characterized by a deficiency of arginine vasopressin.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ?g. }
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- NP681617.RA2Gi8jPzIVFGWGMQrMeKgSQPdiWhfNu_XOg64y-AYrDY130_assertion description "[Familial central diabetes insipidus is an inherited disease of predominant autosomal dominant trait characterized by a deficiency of arginine vasopressin.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP681617.RA2Gi8jPzIVFGWGMQrMeKgSQPdiWhfNu_XOg64y-AYrDY130_provenance.
- NP257751.RAwwLMnzZXb2-vw8mmgWA2aUkQqVjvdbhJsAViAB6GTz0130_assertion description "[Familial central diabetes insipidus is an inherited disease of predominant autosomal dominant trait characterized by a deficiency of arginine vasopressin.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP257751.RAwwLMnzZXb2-vw8mmgWA2aUkQqVjvdbhJsAViAB6GTz0130_provenance.