Nanopublications LDF server

Matches in Nanopublications for { ?s ?p "[Deficiencies in fatty acid metabolism have been extensively studied in cases of SIDS, and by far the most well-investigated mutation is the A985G mutation in the medium-chain acyl-CoA dehydrogenase (MCAD) gene, which is the most prevalent mutation causing MCAD deficiency.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ?g. }

• assertion description "[Deficiencies in fatty acid metabolism have been extensively studied in cases of SIDS, and by far the most well-investigated mutation is the A985G mutation in the medium-chain acyl-CoA dehydrogenase (MCAD) gene, which is the most prevalent mutation causing MCAD deficiency.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
• NP446224.RAUGEjSwr7BLtk_oB1Xx5hUJ8IVqS_BnOv5n2_jGxQduE130_assertion description "[Deficiencies in fatty acid metabolism have been extensively studied in cases of SIDS, and by far the most well-investigated mutation is the A985G mutation in the medium-chain acyl-CoA dehydrogenase (MCAD) gene, which is the most prevalent mutation causing MCAD deficiency.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP446224.RAUGEjSwr7BLtk_oB1Xx5hUJ8IVqS_BnOv5n2_jGxQduE130_provenance.
• NP258673.RA8MHpZ8d30TTTe4afa4rr9tFDJ-3smNGLv-0MmtQfFnw130_assertion description "[Deficiencies in fatty acid metabolism have been extensively studied in cases of SIDS, and by far the most well-investigated mutation is the A985G mutation in the medium-chain acyl-CoA dehydrogenase (MCAD) gene, which is the most prevalent mutation causing MCAD deficiency.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP258673.RA8MHpZ8d30TTTe4afa4rr9tFDJ-3smNGLv-0MmtQfFnw130_provenance.
• assertion description "[Deficiencies in fatty acid metabolism have been extensively studied in cases of SIDS, and by far the most well-investigated mutation is the A985G mutation in the medium-chain acyl-CoA dehydrogenase (MCAD) gene, which is the most prevalent mutation causing MCAD deficiency.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
• NP463020.RAX1_Z0oZEwRzy0Mi7fQM5TYFPlmDf6O93xBosTl49oo0130_assertion description "[Deficiencies in fatty acid metabolism have been extensively studied in cases of SIDS, and by far the most well-investigated mutation is the A985G mutation in the medium-chain acyl-CoA dehydrogenase (MCAD) gene, which is the most prevalent mutation causing MCAD deficiency.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP463020.RAX1_Z0oZEwRzy0Mi7fQM5TYFPlmDf6O93xBosTl49oo0130_provenance.
• NP300447.RADmMM94MrKIGmcMG-O7nxRAaukKmwl6uizC9jT_Lkm0Y130_assertion description "[Deficiencies in fatty acid metabolism have been extensively studied in cases of SIDS, and by far the most well-investigated mutation is the A985G mutation in the medium-chain acyl-CoA dehydrogenase (MCAD) gene, which is the most prevalent mutation causing MCAD deficiency.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP300447.RADmMM94MrKIGmcMG-O7nxRAaukKmwl6uizC9jT_Lkm0Y130_provenance.
• NP463021.RArcu2DByz_1-iQY_Upk_Ku5vBhiykN3ZI7zQ1gb_Mgmg130_assertion description "[Deficiencies in fatty acid metabolism have been extensively studied in cases of SIDS, and by far the most well-investigated mutation is the A985G mutation in the medium-chain acyl-CoA dehydrogenase (MCAD) gene, which is the most prevalent mutation causing MCAD deficiency.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP463021.RArcu2DByz_1-iQY_Upk_Ku5vBhiykN3ZI7zQ1gb_Mgmg130_provenance.
• NP463022.RAtYRde2qAOeOumstz2nlLCsYO1T2XBfFlVWwr7rIgrzI130_assertion description "[Deficiencies in fatty acid metabolism have been extensively studied in cases of SIDS, and by far the most well-investigated mutation is the A985G mutation in the medium-chain acyl-CoA dehydrogenase (MCAD) gene, which is the most prevalent mutation causing MCAD deficiency.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP463022.RAtYRde2qAOeOumstz2nlLCsYO1T2XBfFlVWwr7rIgrzI130_provenance.
• NP220356.RA4KxR6MZkxdGwhuRT3U-pdZR_yL4xTszMxPT9FCItBvA130_assertion description "[Deficiencies in fatty acid metabolism have been extensively studied in cases of SIDS, and by far the most well-investigated mutation is the A985G mutation in the medium-chain acyl-CoA dehydrogenase (MCAD) gene, which is the most prevalent mutation causing MCAD deficiency.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP220356.RA4KxR6MZkxdGwhuRT3U-pdZR_yL4xTszMxPT9FCItBvA130_provenance.
• NP300437.RAwbaR58ZZUw_kbkkQpnJkPrESB1HHIII3L9y9OzSiy5s130_assertion description "[Deficiencies in fatty acid metabolism have been extensively studied in cases of SIDS, and by far the most well-investigated mutation is the A985G mutation in the medium-chain acyl-CoA dehydrogenase (MCAD) gene, which is the most prevalent mutation causing MCAD deficiency.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP300437.RAwbaR58ZZUw_kbkkQpnJkPrESB1HHIII3L9y9OzSiy5s130_provenance.
• NP220351.RAM9DXYUdc_-s4ojnTBMKD_lIA4XXh-x0eq3RUyxYzWdg130_assertion description "[Deficiencies in fatty acid metabolism have been extensively studied in cases of SIDS, and by far the most well-investigated mutation is the A985G mutation in the medium-chain acyl-CoA dehydrogenase (MCAD) gene, which is the most prevalent mutation causing MCAD deficiency.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP220351.RAM9DXYUdc_-s4ojnTBMKD_lIA4XXh-x0eq3RUyxYzWdg130_provenance.
• NP463019.RAIM2A-ntJnDxBtMB1mjFJDAL9RxIYDOEUKWoZLCxRQKE130_assertion description "[Deficiencies in fatty acid metabolism have been extensively studied in cases of SIDS, and by far the most well-investigated mutation is the A985G mutation in the medium-chain acyl-CoA dehydrogenase (MCAD) gene, which is the most prevalent mutation causing MCAD deficiency.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP463019.RAIM2A-ntJnDxBtMB1mjFJDAL9RxIYDOEUKWoZLCxRQKE130_provenance.