Matches in Nanopublications for { ?s ?p "[Congenital nephrogenic diabetes insipidus (NDI) is a rare disease caused most often by mutations in the vasopressin V2 receptor (AVPR2).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ?g. }
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- NP900024.RAfN0Xc3WN9GAZceldh2Kvff5qycWskO1Aq9RUTRIRY68130_assertion description "[Congenital nephrogenic diabetes insipidus (NDI) is a rare disease caused most often by mutations in the vasopressin V2 receptor (AVPR2).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP900024.RAfN0Xc3WN9GAZceldh2Kvff5qycWskO1Aq9RUTRIRY68130_provenance.
- assertion description "[Congenital nephrogenic diabetes insipidus (NDI) is a rare disease caused most often by mutations in the vasopressin V2 receptor (AVPR2).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
- assertion description "[Congenital nephrogenic diabetes insipidus (NDI) is a rare disease caused most often by mutations in the vasopressin V2 receptor (AVPR2).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
- NP1380694.RADdrx00LRIWQ4W3L5uHfM6aOuvgEMvfDCFXalI2-16zc130_assertion description "[Congenital nephrogenic diabetes insipidus (NDI) is a rare disease caused most often by mutations in the vasopressin V2 receptor (AVPR2).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1380694.RADdrx00LRIWQ4W3L5uHfM6aOuvgEMvfDCFXalI2-16zc130_provenance.
- NP1380695.RAnwGA57A-qML2-_2zrKptueMrwk5O1zyZKNVC_hNzMGY130_assertion description "[Congenital nephrogenic diabetes insipidus (NDI) is a rare disease caused most often by mutations in the vasopressin V2 receptor (AVPR2).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1380695.RAnwGA57A-qML2-_2zrKptueMrwk5O1zyZKNVC_hNzMGY130_provenance.
- NP258146.RA4qNwpIA1BXe-ZqvmkIxjWxqMt-aw588Jh3emZwx23Gg130_assertion description "[Congenital nephrogenic diabetes insipidus (NDI) is a rare disease caused most often by mutations in the vasopressin V2 receptor (AVPR2).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP258146.RA4qNwpIA1BXe-ZqvmkIxjWxqMt-aw588Jh3emZwx23Gg130_provenance.