Nanopublications LDF server

Matches in Nanopublications for { ?s ?p "[Rare forms of congenital hyperinsulinism (CHI) are caused by mutations in GLUD1 (encoding glutamate dehydrogenase), GCK (encoding glucokinase), HADH (encoding for L-3-hydroxyacyl-CoA dehydrogenase), SLC16A1 (encoding the monocarboxylat transporter 1), HNF4A (encoding hepatocyte nuclear factor 4?) or UCP2 (encoding mitochondrial uncoupling protein 2).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ?g. }

• NP767037.RAjfL2UNyOwx7CsZAG2EhC8eluwsqVAtBT-2NlinCsUwY130_assertion description "[Rare forms of congenital hyperinsulinism (CHI) are caused by mutations in GLUD1 (encoding glutamate dehydrogenase), GCK (encoding glucokinase), HADH (encoding for L-3-hydroxyacyl-CoA dehydrogenase), SLC16A1 (encoding the monocarboxylat transporter 1), HNF4A (encoding hepatocyte nuclear factor 4?) or UCP2 (encoding mitochondrial uncoupling protein 2).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP767037.RAjfL2UNyOwx7CsZAG2EhC8eluwsqVAtBT-2NlinCsUwY130_provenance.
• NP230486.RAbeZb93MdikgrDibAcS_IjkSRc9pxrBVuW1Job-8ulo8130_assertion description "[Rare forms of congenital hyperinsulinism (CHI) are caused by mutations in GLUD1 (encoding glutamate dehydrogenase), GCK (encoding glucokinase), HADH (encoding for L-3-hydroxyacyl-CoA dehydrogenase), SLC16A1 (encoding the monocarboxylat transporter 1), HNF4A (encoding hepatocyte nuclear factor 4?) or UCP2 (encoding mitochondrial uncoupling protein 2).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP230486.RAbeZb93MdikgrDibAcS_IjkSRc9pxrBVuW1Job-8ulo8130_provenance.
• NP422979.RAn5o-viMwZ_7l9Ob42m7KFzCYpM3sfD3YNaTyZE2MPpo130_assertion description "[Rare forms of congenital hyperinsulinism (CHI) are caused by mutations in GLUD1 (encoding glutamate dehydrogenase), GCK (encoding glucokinase), HADH (encoding for L-3-hydroxyacyl-CoA dehydrogenase), SLC16A1 (encoding the monocarboxylat transporter 1), HNF4A (encoding hepatocyte nuclear factor 4?) or UCP2 (encoding mitochondrial uncoupling protein 2).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP422979.RAn5o-viMwZ_7l9Ob42m7KFzCYpM3sfD3YNaTyZE2MPpo130_provenance.
• NP882610.RAhpFB6W6kA3nHtHVyViL8gY-fzOGEuQARh9MUNFE1nug130_assertion description "[Rare forms of congenital hyperinsulinism (CHI) are caused by mutations in GLUD1 (encoding glutamate dehydrogenase), GCK (encoding glucokinase), HADH (encoding for L-3-hydroxyacyl-CoA dehydrogenase), SLC16A1 (encoding the monocarboxylat transporter 1), HNF4A (encoding hepatocyte nuclear factor 4?) or UCP2 (encoding mitochondrial uncoupling protein 2).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP882610.RAhpFB6W6kA3nHtHVyViL8gY-fzOGEuQARh9MUNFE1nug130_provenance.
• NP330391.RA6dcMdsR80RCiuvkbV3apyIphkitA14NVD1fe9JcRwOY130_assertion description "[Rare forms of congenital hyperinsulinism (CHI) are caused by mutations in GLUD1 (encoding glutamate dehydrogenase), GCK (encoding glucokinase), HADH (encoding for L-3-hydroxyacyl-CoA dehydrogenase), SLC16A1 (encoding the monocarboxylat transporter 1), HNF4A (encoding hepatocyte nuclear factor 4?) or UCP2 (encoding mitochondrial uncoupling protein 2).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP330391.RA6dcMdsR80RCiuvkbV3apyIphkitA14NVD1fe9JcRwOY130_provenance.
• NP938463.RAy9BLX36t9t3ZIpbYRs6-c0vlv45__oARym6srkUi-Kg130_assertion description "[Rare forms of congenital hyperinsulinism (CHI) are caused by mutations in GLUD1 (encoding glutamate dehydrogenase), GCK (encoding glucokinase), HADH (encoding for L-3-hydroxyacyl-CoA dehydrogenase), SLC16A1 (encoding the monocarboxylat transporter 1), HNF4A (encoding hepatocyte nuclear factor 4?) or UCP2 (encoding mitochondrial uncoupling protein 2).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP938463.RAy9BLX36t9t3ZIpbYRs6-c0vlv45__oARym6srkUi-Kg130_provenance.
• NP683808.RA-vHkUrI8uxw_3L4SWR9BuDgfC8E9vYgpnIgbKwxq9CI130_assertion description "[Rare forms of congenital hyperinsulinism (CHI) are caused by mutations in GLUD1 (encoding glutamate dehydrogenase), GCK (encoding glucokinase), HADH (encoding for L-3-hydroxyacyl-CoA dehydrogenase), SLC16A1 (encoding the monocarboxylat transporter 1), HNF4A (encoding hepatocyte nuclear factor 4?) or UCP2 (encoding mitochondrial uncoupling protein 2).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP683808.RA-vHkUrI8uxw_3L4SWR9BuDgfC8E9vYgpnIgbKwxq9CI130_provenance.
• NP748852.RAFpMGGIWvhHUUa8MMdGFpGqUxkX3QqQdsY2uCIbHVrHQ130_assertion description "[Rare forms of congenital hyperinsulinism (CHI) are caused by mutations in GLUD1 (encoding glutamate dehydrogenase), GCK (encoding glucokinase), HADH (encoding for L-3-hydroxyacyl-CoA dehydrogenase), SLC16A1 (encoding the monocarboxylat transporter 1), HNF4A (encoding hepatocyte nuclear factor 4?) or UCP2 (encoding mitochondrial uncoupling protein 2).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP748852.RAFpMGGIWvhHUUa8MMdGFpGqUxkX3QqQdsY2uCIbHVrHQ130_provenance.
• NP429052.RAAICf7y5ShbNz4x5zc2j-b38PuiYX2Sg9p27kKoOiLsk130_assertion description "[Rare forms of congenital hyperinsulinism (CHI) are caused by mutations in GLUD1 (encoding glutamate dehydrogenase), GCK (encoding glucokinase), HADH (encoding for L-3-hydroxyacyl-CoA dehydrogenase), SLC16A1 (encoding the monocarboxylat transporter 1), HNF4A (encoding hepatocyte nuclear factor 4?) or UCP2 (encoding mitochondrial uncoupling protein 2).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP429052.RAAICf7y5ShbNz4x5zc2j-b38PuiYX2Sg9p27kKoOiLsk130_provenance.
• NP433912.RAvABNm7fNzEhFy8hqxarhRHVcj6fNDB_DVafztyOGvvA130_assertion description "[Rare forms of congenital hyperinsulinism (CHI) are caused by mutations in GLUD1 (encoding glutamate dehydrogenase), GCK (encoding glucokinase), HADH (encoding for L-3-hydroxyacyl-CoA dehydrogenase), SLC16A1 (encoding the monocarboxylat transporter 1), HNF4A (encoding hepatocyte nuclear factor 4?) or UCP2 (encoding mitochondrial uncoupling protein 2).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP433912.RAvABNm7fNzEhFy8hqxarhRHVcj6fNDB_DVafztyOGvvA130_provenance.
• NP443213.RAgjoqi4F2w7573jkaFoX4kRT7EQyxlSp7FF0_YvukuLY130_assertion description "[Rare forms of congenital hyperinsulinism (CHI) are caused by mutations in GLUD1 (encoding glutamate dehydrogenase), GCK (encoding glucokinase), HADH (encoding for L-3-hydroxyacyl-CoA dehydrogenase), SLC16A1 (encoding the monocarboxylat transporter 1), HNF4A (encoding hepatocyte nuclear factor 4?) or UCP2 (encoding mitochondrial uncoupling protein 2).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP443213.RAgjoqi4F2w7573jkaFoX4kRT7EQyxlSp7FF0_YvukuLY130_provenance.
• NP443244.RAkIUNRz3G12KJ-qMTgvPXkhO98IfmWGi1tfDOR3hHf0s130_assertion description "[Rare forms of congenital hyperinsulinism (CHI) are caused by mutations in GLUD1 (encoding glutamate dehydrogenase), GCK (encoding glucokinase), HADH (encoding for L-3-hydroxyacyl-CoA dehydrogenase), SLC16A1 (encoding the monocarboxylat transporter 1), HNF4A (encoding hepatocyte nuclear factor 4?) or UCP2 (encoding mitochondrial uncoupling protein 2).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP443244.RAkIUNRz3G12KJ-qMTgvPXkhO98IfmWGi1tfDOR3hHf0s130_provenance.
• NP461584.RA7PlKNkdsWS6cHR-dYlxy1UBQewR27B6LviR6ZRT_1xs130_assertion description "[Rare forms of congenital hyperinsulinism (CHI) are caused by mutations in GLUD1 (encoding glutamate dehydrogenase), GCK (encoding glucokinase), HADH (encoding for L-3-hydroxyacyl-CoA dehydrogenase), SLC16A1 (encoding the monocarboxylat transporter 1), HNF4A (encoding hepatocyte nuclear factor 4?) or UCP2 (encoding mitochondrial uncoupling protein 2).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP461584.RA7PlKNkdsWS6cHR-dYlxy1UBQewR27B6LviR6ZRT_1xs130_provenance.