Nanopublications LDF server

Matches in Nanopublications for { ?s ?p "[The protocol was standardized on a variety of known mutations, in 11 patients with cystic fibrosis (CF), Fabry's disease (FD), steroid 21-hydroxylase deficiency (21-HD) and Duchenne/Becker muscular dystrophy (DMD/BMD).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ?g. }

• NP208607.RApKdm0Ax-Rn3gzDc-g2hjvYlX4P4G7lXrcrSOcfZQ254130_assertion description "[The protocol was standardized on a variety of known mutations, in 11 patients with cystic fibrosis (CF), Fabry's disease (FD), steroid 21-hydroxylase deficiency (21-HD) and Duchenne/Becker muscular dystrophy (DMD/BMD).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP208607.RApKdm0Ax-Rn3gzDc-g2hjvYlX4P4G7lXrcrSOcfZQ254130_provenance.
• NP399610.RAse3_RMSYe08IjvB9zQwaktD9v1lFYH-wLoCflW5mevA130_assertion description "[The protocol was standardized on a variety of known mutations, in 11 patients with cystic fibrosis (CF), Fabry's disease (FD), steroid 21-hydroxylase deficiency (21-HD) and Duchenne/Becker muscular dystrophy (DMD/BMD).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP399610.RAse3_RMSYe08IjvB9zQwaktD9v1lFYH-wLoCflW5mevA130_provenance.
• NP528339.RAs_ElC5YnfLiiHD6Skq8bLwHl9G6cIp5exSlZefQhtek130_assertion description "[The protocol was standardized on a variety of known mutations, in 11 patients with cystic fibrosis (CF), Fabry's disease (FD), steroid 21-hydroxylase deficiency (21-HD) and Duchenne/Becker muscular dystrophy (DMD/BMD).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP528339.RAs_ElC5YnfLiiHD6Skq8bLwHl9G6cIp5exSlZefQhtek130_provenance.
• NP164199.RAsw20rkj_j-OlKagtXliRPE3Is_llqvHGY4aItYPRfx0130_assertion description "[The protocol was standardized on a variety of known mutations, in 11 patients with cystic fibrosis (CF), Fabry's disease (FD), steroid 21-hydroxylase deficiency (21-HD) and Duchenne/Becker muscular dystrophy (DMD/BMD).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP164199.RAsw20rkj_j-OlKagtXliRPE3Is_llqvHGY4aItYPRfx0130_provenance.
• NP696543.RAuNyo3doL1T-hs6yr5II1uG7e2KdNxcj6ECKpSmLyNjE130_assertion description "[The protocol was standardized on a variety of known mutations, in 11 patients with cystic fibrosis (CF), Fabry's disease (FD), steroid 21-hydroxylase deficiency (21-HD) and Duchenne/Becker muscular dystrophy (DMD/BMD).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP696543.RAuNyo3doL1T-hs6yr5II1uG7e2KdNxcj6ECKpSmLyNjE130_provenance.
• NP784213.RApVtDVav4-oL-Q9cYeAhUy1BH8an-AhD2MCeaJ1aLKFI130_assertion description "[The protocol was standardized on a variety of known mutations, in 11 patients with cystic fibrosis (CF), Fabry's disease (FD), steroid 21-hydroxylase deficiency (21-HD) and Duchenne/Becker muscular dystrophy (DMD/BMD).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP784213.RApVtDVav4-oL-Q9cYeAhUy1BH8an-AhD2MCeaJ1aLKFI130_provenance.
• NP807689.RArxUCuk4RQQBHHV7WG-bqoo4GUW9oHyR1LT8lN_oUBq0130_assertion description "[The protocol was standardized on a variety of known mutations, in 11 patients with cystic fibrosis (CF), Fabry's disease (FD), steroid 21-hydroxylase deficiency (21-HD) and Duchenne/Becker muscular dystrophy (DMD/BMD).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP807689.RArxUCuk4RQQBHHV7WG-bqoo4GUW9oHyR1LT8lN_oUBq0130_provenance.
• NP441180.RAKp_EiiDUl8xNECgNi1ZAkNJqoEvXgzj4-QJ0Ybh6ias130_assertion description "[The protocol was standardized on a variety of known mutations, in 11 patients with cystic fibrosis (CF), Fabry's disease (FD), steroid 21-hydroxylase deficiency (21-HD) and Duchenne/Becker muscular dystrophy (DMD/BMD).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP441180.RAKp_EiiDUl8xNECgNi1ZAkNJqoEvXgzj4-QJ0Ybh6ias130_provenance.
• NP475184.RAXrAI-ba6V5XDHlHW3XGZZbBJI6wYAHBgb5iMNrEuOtI130_assertion description "[The protocol was standardized on a variety of known mutations, in 11 patients with cystic fibrosis (CF), Fabry's disease (FD), steroid 21-hydroxylase deficiency (21-HD) and Duchenne/Becker muscular dystrophy (DMD/BMD).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP475184.RAXrAI-ba6V5XDHlHW3XGZZbBJI6wYAHBgb5iMNrEuOtI130_provenance.
• NP430184.RA2h0QLBdPYBs590f0gg-d31_6cJs6dTxvZgYskWqLx5g130_assertion description "[The protocol was standardized on a variety of known mutations, in 11 patients with cystic fibrosis (CF), Fabry's disease (FD), steroid 21-hydroxylase deficiency (21-HD) and Duchenne/Becker muscular dystrophy (DMD/BMD).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP430184.RA2h0QLBdPYBs590f0gg-d31_6cJs6dTxvZgYskWqLx5g130_provenance.
• NP355240.RAYsP3S6xYm3ymjaYMGkK_Rqq8E56Dzp8rLtv2UufvtPM130_assertion description "[The protocol was standardized on a variety of known mutations, in 11 patients with cystic fibrosis (CF), Fabry's disease (FD), steroid 21-hydroxylase deficiency (21-HD) and Duchenne/Becker muscular dystrophy (DMD/BMD).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP355240.RAYsP3S6xYm3ymjaYMGkK_Rqq8E56Dzp8rLtv2UufvtPM130_provenance.
• NP802123.RAxQHsbj4M8_M0OkdHIgYyf7IeNXfduyBbH2SzlCYJHig130_assertion description "[The protocol was standardized on a variety of known mutations, in 11 patients with cystic fibrosis (CF), Fabry's disease (FD), steroid 21-hydroxylase deficiency (21-HD) and Duchenne/Becker muscular dystrophy (DMD/BMD).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP802123.RAxQHsbj4M8_M0OkdHIgYyf7IeNXfduyBbH2SzlCYJHig130_provenance.
• NP775429.RAvPTNdYFDLHo7AxKkZN8t-HoZZxXQmBlUAP0Hh1EzkwM130_assertion description "[The protocol was standardized on a variety of known mutations, in 11 patients with cystic fibrosis (CF), Fabry's disease (FD), steroid 21-hydroxylase deficiency (21-HD) and Duchenne/Becker muscular dystrophy (DMD/BMD).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP775429.RAvPTNdYFDLHo7AxKkZN8t-HoZZxXQmBlUAP0Hh1EzkwM130_provenance.
• NP775489.RApHMVUB6_zc89bkInPDfq0NtO4Bru3YaP1-5MVmdX3dE130_assertion description "[The protocol was standardized on a variety of known mutations, in 11 patients with cystic fibrosis (CF), Fabry's disease (FD), steroid 21-hydroxylase deficiency (21-HD) and Duchenne/Becker muscular dystrophy (DMD/BMD).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP775489.RApHMVUB6_zc89bkInPDfq0NtO4Bru3YaP1-5MVmdX3dE130_provenance.
• NP636675.RASQ08j7on4A1-e8dgkSHLQQcC8IGMndWk6gIJJk_vPLc130_assertion description "[The protocol was standardized on a variety of known mutations, in 11 patients with cystic fibrosis (CF), Fabry's disease (FD), steroid 21-hydroxylase deficiency (21-HD) and Duchenne/Becker muscular dystrophy (DMD/BMD).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP636675.RASQ08j7on4A1-e8dgkSHLQQcC8IGMndWk6gIJJk_vPLc130_provenance.
• NP636679.RAQvJSqTccnBmRmEQU1bIAK-hSR7ldT3OuDrzRKYaAmLQ130_assertion description "[The protocol was standardized on a variety of known mutations, in 11 patients with cystic fibrosis (CF), Fabry's disease (FD), steroid 21-hydroxylase deficiency (21-HD) and Duchenne/Becker muscular dystrophy (DMD/BMD).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP636679.RAQvJSqTccnBmRmEQU1bIAK-hSR7ldT3OuDrzRKYaAmLQ130_provenance.
• NP636681.RAVnDWxntWloqFHkEL1ohMgEe0AQjO6-cztso35xZvZhI130_assertion description "[The protocol was standardized on a variety of known mutations, in 11 patients with cystic fibrosis (CF), Fabry's disease (FD), steroid 21-hydroxylase deficiency (21-HD) and Duchenne/Becker muscular dystrophy (DMD/BMD).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP636681.RAVnDWxntWloqFHkEL1ohMgEe0AQjO6-cztso35xZvZhI130_provenance.
• NP892333.RAF9OUJMOLbi8yKHbKlMd9VJUdU-L16C2Ef2pY6OAqaAo130_assertion description "[The protocol was standardized on a variety of known mutations, in 11 patients with cystic fibrosis (CF), Fabry's disease (FD), steroid 21-hydroxylase deficiency (21-HD) and Duchenne/Becker muscular dystrophy (DMD/BMD).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP892333.RAF9OUJMOLbi8yKHbKlMd9VJUdU-L16C2Ef2pY6OAqaAo130_provenance.
• NP636678.RApXC6fMBXNCAckRZpk66o9l5PIk9cKVRKYVXNDiqwBiA130_assertion description "[The protocol was standardized on a variety of known mutations, in 11 patients with cystic fibrosis (CF), Fabry's disease (FD), steroid 21-hydroxylase deficiency (21-HD) and Duchenne/Becker muscular dystrophy (DMD/BMD).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP636678.RApXC6fMBXNCAckRZpk66o9l5PIk9cKVRKYVXNDiqwBiA130_provenance.
• NP636680.RAsKf8NVRDUTqhWlpZckCefsqXC0Ij97hyDPuvg4kuao4130_assertion description "[The protocol was standardized on a variety of known mutations, in 11 patients with cystic fibrosis (CF), Fabry's disease (FD), steroid 21-hydroxylase deficiency (21-HD) and Duchenne/Becker muscular dystrophy (DMD/BMD).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP636680.RAsKf8NVRDUTqhWlpZckCefsqXC0Ij97hyDPuvg4kuao4130_provenance.
• NP636682.RArKh6k10EaPiR1Hr1ahbBaV7OUjMGZCZ_dArh4nGuNiw130_assertion description "[The protocol was standardized on a variety of known mutations, in 11 patients with cystic fibrosis (CF), Fabry's disease (FD), steroid 21-hydroxylase deficiency (21-HD) and Duchenne/Becker muscular dystrophy (DMD/BMD).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP636682.RArKh6k10EaPiR1Hr1ahbBaV7OUjMGZCZ_dArh4nGuNiw130_provenance.
• NP355600.RAI2kM4LhcNZFFw1fLpRtobqMuU17CltPTNATVkUdHmF4130_assertion description "[The protocol was standardized on a variety of known mutations, in 11 patients with cystic fibrosis (CF), Fabry's disease (FD), steroid 21-hydroxylase deficiency (21-HD) and Duchenne/Becker muscular dystrophy (DMD/BMD).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP355600.RAI2kM4LhcNZFFw1fLpRtobqMuU17CltPTNATVkUdHmF4130_provenance.
• NP355670.RAOtobL_eeI68yhd4JoB_ByWjgWpGMPseVcbHFOz76huY130_assertion description "[The protocol was standardized on a variety of known mutations, in 11 patients with cystic fibrosis (CF), Fabry's disease (FD), steroid 21-hydroxylase deficiency (21-HD) and Duchenne/Becker muscular dystrophy (DMD/BMD).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP355670.RAOtobL_eeI68yhd4JoB_ByWjgWpGMPseVcbHFOz76huY130_provenance.
• NP775266.RAGNQA4VyZn51qMMHwBIO8zvKiANf2gynvcLy9e-7Em9Y130_assertion description "[The protocol was standardized on a variety of known mutations, in 11 patients with cystic fibrosis (CF), Fabry's disease (FD), steroid 21-hydroxylase deficiency (21-HD) and Duchenne/Becker muscular dystrophy (DMD/BMD).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP775266.RAGNQA4VyZn51qMMHwBIO8zvKiANf2gynvcLy9e-7Em9Y130_provenance.
• NP636676.RA1oNpBts9u8RQ4DaqUYmSZZ2MoOuUremF_a1yp_RJUWI130_assertion description "[The protocol was standardized on a variety of known mutations, in 11 patients with cystic fibrosis (CF), Fabry's disease (FD), steroid 21-hydroxylase deficiency (21-HD) and Duchenne/Becker muscular dystrophy (DMD/BMD).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP636676.RA1oNpBts9u8RQ4DaqUYmSZZ2MoOuUremF_a1yp_RJUWI130_provenance.
• NP636677.RA4BXA_rXLoxJAfXrQNoFTPpNIpJuFJ9Hh-x2CnSUN-nA130_assertion description "[The protocol was standardized on a variety of known mutations, in 11 patients with cystic fibrosis (CF), Fabry's disease (FD), steroid 21-hydroxylase deficiency (21-HD) and Duchenne/Becker muscular dystrophy (DMD/BMD).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP636677.RA4BXA_rXLoxJAfXrQNoFTPpNIpJuFJ9Hh-x2CnSUN-nA130_provenance.