Nanopublications LDF server

Matches in Nanopublications for { ?s ?p "[In about a decade, mutations in 8 different genes (IPF1, EIF2AK3, GK, FOXP3, KCNJ11, ABCC8, PTF1A and GLIS3) have been discovered in patients with the permanent form of the disease, and 3 genetic abnormalities (defects in the paternally imprinted chromosomal region 6q24 and 'mild' activating mutations in KCNJ11 or ABCC8) have been detected in subjects with transient neonatal diabetes.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ?g. }

• NP812830.RAVUR9_MMP2hRXpjZpLhptMT0pHNSMkp88V3lGwj75quo130_assertion description "[In about a decade, mutations in 8 different genes (IPF1, EIF2AK3, GK, FOXP3, KCNJ11, ABCC8, PTF1A and GLIS3) have been discovered in patients with the permanent form of the disease, and 3 genetic abnormalities (defects in the paternally imprinted chromosomal region 6q24 and 'mild' activating mutations in KCNJ11 or ABCC8) have been detected in subjects with transient neonatal diabetes.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP812830.RAVUR9_MMP2hRXpjZpLhptMT0pHNSMkp88V3lGwj75quo130_provenance.
• NP259515.RAhCvOuiQVTrRFsJInNJL9GMpkGazhfhRVvOoPEh1cNrM130_assertion description "[In about a decade, mutations in 8 different genes (IPF1, EIF2AK3, GK, FOXP3, KCNJ11, ABCC8, PTF1A and GLIS3) have been discovered in patients with the permanent form of the disease, and 3 genetic abnormalities (defects in the paternally imprinted chromosomal region 6q24 and 'mild' activating mutations in KCNJ11 or ABCC8) have been detected in subjects with transient neonatal diabetes.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP259515.RAhCvOuiQVTrRFsJInNJL9GMpkGazhfhRVvOoPEh1cNrM130_provenance.
• NP724978.RAw8p47DRGRRBFwMijSum_2MX_nXowpHTpfSecT74t_fU130_assertion description "[In about a decade, mutations in 8 different genes (IPF1, EIF2AK3, GK, FOXP3, KCNJ11, ABCC8, PTF1A and GLIS3) have been discovered in patients with the permanent form of the disease, and 3 genetic abnormalities (defects in the paternally imprinted chromosomal region 6q24 and 'mild' activating mutations in KCNJ11 or ABCC8) have been detected in subjects with transient neonatal diabetes.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP724978.RAw8p47DRGRRBFwMijSum_2MX_nXowpHTpfSecT74t_fU130_provenance.
• NP457854.RAKX4OrcNqFQVCQ8l5aKsDqZzZGYiPRsqtv02MyaDgQvA130_assertion description "[In about a decade, mutations in 8 different genes (IPF1, EIF2AK3, GK, FOXP3, KCNJ11, ABCC8, PTF1A and GLIS3) have been discovered in patients with the permanent form of the disease, and 3 genetic abnormalities (defects in the paternally imprinted chromosomal region 6q24 and 'mild' activating mutations in KCNJ11 or ABCC8) have been detected in subjects with transient neonatal diabetes.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP457854.RAKX4OrcNqFQVCQ8l5aKsDqZzZGYiPRsqtv02MyaDgQvA130_provenance.
• NP981969.RADsirB21RQUK3dkzcTGTA5aAZVhYf5WsAP5z5_qmb3kQ130_assertion description "[In about a decade, mutations in 8 different genes (IPF1, EIF2AK3, GK, FOXP3, KCNJ11, ABCC8, PTF1A and GLIS3) have been discovered in patients with the permanent form of the disease, and 3 genetic abnormalities (defects in the paternally imprinted chromosomal region 6q24 and 'mild' activating mutations in KCNJ11 or ABCC8) have been detected in subjects with transient neonatal diabetes.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP981969.RADsirB21RQUK3dkzcTGTA5aAZVhYf5WsAP5z5_qmb3kQ130_provenance.
• NP639142.RAANmhDq_XtQ4N-iKsaFKYPCoNvJiD8ok9DdI4Dy_XH14130_assertion description "[In about a decade, mutations in 8 different genes (IPF1, EIF2AK3, GK, FOXP3, KCNJ11, ABCC8, PTF1A and GLIS3) have been discovered in patients with the permanent form of the disease, and 3 genetic abnormalities (defects in the paternally imprinted chromosomal region 6q24 and 'mild' activating mutations in KCNJ11 or ABCC8) have been detected in subjects with transient neonatal diabetes.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP639142.RAANmhDq_XtQ4N-iKsaFKYPCoNvJiD8ok9DdI4Dy_XH14130_provenance.
• NP639143.RAAPQk899Ue5KkPddXqVkdTs1bnChVw7WvfiVp6EMOg6s130_assertion description "[In about a decade, mutations in 8 different genes (IPF1, EIF2AK3, GK, FOXP3, KCNJ11, ABCC8, PTF1A and GLIS3) have been discovered in patients with the permanent form of the disease, and 3 genetic abnormalities (defects in the paternally imprinted chromosomal region 6q24 and 'mild' activating mutations in KCNJ11 or ABCC8) have been detected in subjects with transient neonatal diabetes.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP639143.RAAPQk899Ue5KkPddXqVkdTs1bnChVw7WvfiVp6EMOg6s130_provenance.
• NP639145.RAB-_YdZe_z7O2JVM2o3LiHkIycpC-2hlIJ2jpyUQQvm0130_assertion description "[In about a decade, mutations in 8 different genes (IPF1, EIF2AK3, GK, FOXP3, KCNJ11, ABCC8, PTF1A and GLIS3) have been discovered in patients with the permanent form of the disease, and 3 genetic abnormalities (defects in the paternally imprinted chromosomal region 6q24 and 'mild' activating mutations in KCNJ11 or ABCC8) have been detected in subjects with transient neonatal diabetes.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP639145.RAB-_YdZe_z7O2JVM2o3LiHkIycpC-2hlIJ2jpyUQQvm0130_provenance.
• NP685964.RAPQR_qx50CjyGP7oEI7iSOmRQ0ItngqLqzVIObyBstyM130_assertion description "[In about a decade, mutations in 8 different genes (IPF1, EIF2AK3, GK, FOXP3, KCNJ11, ABCC8, PTF1A and GLIS3) have been discovered in patients with the permanent form of the disease, and 3 genetic abnormalities (defects in the paternally imprinted chromosomal region 6q24 and 'mild' activating mutations in KCNJ11 or ABCC8) have been detected in subjects with transient neonatal diabetes.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP685964.RAPQR_qx50CjyGP7oEI7iSOmRQ0ItngqLqzVIObyBstyM130_provenance.
• NP978055.RAum1F-7KgJ8FKdI6E6oSje3joQ2VJBo7bNNx0GvDqrIU130_assertion description "[In about a decade, mutations in 8 different genes (IPF1, EIF2AK3, GK, FOXP3, KCNJ11, ABCC8, PTF1A and GLIS3) have been discovered in patients with the permanent form of the disease, and 3 genetic abnormalities (defects in the paternally imprinted chromosomal region 6q24 and 'mild' activating mutations in KCNJ11 or ABCC8) have been detected in subjects with transient neonatal diabetes.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP978055.RAum1F-7KgJ8FKdI6E6oSje3joQ2VJBo7bNNx0GvDqrIU130_provenance.
• NP639144.RAwBJA27Z3iOo8GuSyP2ConsW3D5h7Pdu3vVVbvyrKEQ8130_assertion description "[In about a decade, mutations in 8 different genes (IPF1, EIF2AK3, GK, FOXP3, KCNJ11, ABCC8, PTF1A and GLIS3) have been discovered in patients with the permanent form of the disease, and 3 genetic abnormalities (defects in the paternally imprinted chromosomal region 6q24 and 'mild' activating mutations in KCNJ11 or ABCC8) have been detected in subjects with transient neonatal diabetes.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP639144.RAwBJA27Z3iOo8GuSyP2ConsW3D5h7Pdu3vVVbvyrKEQ8130_provenance.