Matches in Nanopublications for { ?s ?p "[Autosomal dominant familial neurohypophyseal diabetes insipidus (adFNDI), a disorder caused by mutations in the vasopressin (AVP)-neurophysin II (NPII) gene, manifests gradually during early childhood with progressive polyuria and polydipsia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ?g. }
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- NP487604.RA6Ld16iHlINTcXVQQZoFZAGP4cuyl8yD8MeK6z-zVSAo130_assertion description "[Autosomal dominant familial neurohypophyseal diabetes insipidus (adFNDI), a disorder caused by mutations in the vasopressin (AVP)-neurophysin II (NPII) gene, manifests gradually during early childhood with progressive polyuria and polydipsia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP487604.RA6Ld16iHlINTcXVQQZoFZAGP4cuyl8yD8MeK6z-zVSAo130_provenance.
- NP615822.RAqejoMEjYl-e9LEqJfP7jqRPn3Ym1ihukVZFUnExxP2E130_assertion description "[Autosomal dominant familial neurohypophyseal diabetes insipidus (adFNDI), a disorder caused by mutations in the vasopressin (AVP)-neurophysin II (NPII) gene, manifests gradually during early childhood with progressive polyuria and polydipsia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP615822.RAqejoMEjYl-e9LEqJfP7jqRPn3Ym1ihukVZFUnExxP2E130_provenance.
- assertion description "[Autosomal dominant familial neurohypophyseal diabetes insipidus (adFNDI), a disorder caused by mutations in the vasopressin (AVP)-neurophysin II (NPII) gene, manifests gradually during early childhood with progressive polyuria and polydipsia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
- assertion description "[Autosomal dominant familial neurohypophyseal diabetes insipidus (adFNDI), a disorder caused by mutations in the vasopressin (AVP)-neurophysin II (NPII) gene, manifests gradually during early childhood with progressive polyuria and polydipsia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
- NP192363.RAJhDq9k1wrewPHglfRvqvCei615IAnu4hEN3Vf0cw0cA130_assertion description "[Autosomal dominant familial neurohypophyseal diabetes insipidus (adFNDI), a disorder caused by mutations in the vasopressin (AVP)-neurophysin II (NPII) gene, manifests gradually during early childhood with progressive polyuria and polydipsia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP192363.RAJhDq9k1wrewPHglfRvqvCei615IAnu4hEN3Vf0cw0cA130_provenance.
- NP300628.RAxlPlXX13ofcopcxsqKhSxpRLwHYS03tkU5V9LUWqnlc130_assertion description "[Autosomal dominant familial neurohypophyseal diabetes insipidus (adFNDI), a disorder caused by mutations in the vasopressin (AVP)-neurophysin II (NPII) gene, manifests gradually during early childhood with progressive polyuria and polydipsia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP300628.RAxlPlXX13ofcopcxsqKhSxpRLwHYS03tkU5V9LUWqnlc130_provenance.
- NP651673.RA88x0c8sHwZ6q0kpviO7JL0MsuMYN-91_ILreqGtP4u4130_assertion description "[Autosomal dominant familial neurohypophyseal diabetes insipidus (adFNDI), a disorder caused by mutations in the vasopressin (AVP)-neurophysin II (NPII) gene, manifests gradually during early childhood with progressive polyuria and polydipsia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP651673.RA88x0c8sHwZ6q0kpviO7JL0MsuMYN-91_ILreqGtP4u4130_provenance.
- NP704089.RAE3uNkvcZ9YGs0xIZSM5CMfZmVYkOntTgAUmbLN85oeE130_assertion description "[Autosomal dominant familial neurohypophyseal diabetes insipidus (adFNDI), a disorder caused by mutations in the vasopressin (AVP)-neurophysin II (NPII) gene, manifests gradually during early childhood with progressive polyuria and polydipsia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP704089.RAE3uNkvcZ9YGs0xIZSM5CMfZmVYkOntTgAUmbLN85oeE130_provenance.
- NP257818.RAm7pBubUrbBkvMBJoCZm5tN2iqq1kytZiUroUPNTVALk130_assertion description "[Autosomal dominant familial neurohypophyseal diabetes insipidus (adFNDI), a disorder caused by mutations in the vasopressin (AVP)-neurophysin II (NPII) gene, manifests gradually during early childhood with progressive polyuria and polydipsia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP257818.RAm7pBubUrbBkvMBJoCZm5tN2iqq1kytZiUroUPNTVALk130_provenance.
- NP853298.RAYp6imxhmVL_okJmb4x-gbkBVoKT7I1UsWMnr13UxJlk130_assertion description "[Autosomal dominant familial neurohypophyseal diabetes insipidus (adFNDI), a disorder caused by mutations in the vasopressin (AVP)-neurophysin II (NPII) gene, manifests gradually during early childhood with progressive polyuria and polydipsia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP853298.RAYp6imxhmVL_okJmb4x-gbkBVoKT7I1UsWMnr13UxJlk130_provenance.
- NP853299.RAvHNihqA72Qb-P35Hgz4tRmb2K-8MOnXl1qp7H96dCFg130_assertion description "[Autosomal dominant familial neurohypophyseal diabetes insipidus (adFNDI), a disorder caused by mutations in the vasopressin (AVP)-neurophysin II (NPII) gene, manifests gradually during early childhood with progressive polyuria and polydipsia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP853299.RAvHNihqA72Qb-P35Hgz4tRmb2K-8MOnXl1qp7H96dCFg130_provenance.
- NP257799.RA9aPQ_nkNgo19FTm8qWOCITVe2wjk0zP-FgwLjrH_o-E130_assertion description "[Autosomal dominant familial neurohypophyseal diabetes insipidus (adFNDI), a disorder caused by mutations in the vasopressin (AVP)-neurophysin II (NPII) gene, manifests gradually during early childhood with progressive polyuria and polydipsia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP257799.RA9aPQ_nkNgo19FTm8qWOCITVe2wjk0zP-FgwLjrH_o-E130_provenance.