Nanopublications LDF server

Matches in Nanopublications for { ?s ?p "[Spinal muscular atrophy (SMA), the leading genetic cause of death in childhood, is an autosomal recessive neuromuscular disorder characterized by progressive muscle weakness, associated with deletions of the survival motor neuron (SMN) gene identified and mapped to chromosome 5q13.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ?g. }

• NP222055.RASDmjWAKV3nzDySGhysxJ_b_l3e3hKhGlUdIlVRtPQJg130_assertion description "[Spinal muscular atrophy (SMA), the leading genetic cause of death in childhood, is an autosomal recessive neuromuscular disorder characterized by progressive muscle weakness, associated with deletions of the survival motor neuron (SMN) gene identified and mapped to chromosome 5q13.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP222055.RASDmjWAKV3nzDySGhysxJ_b_l3e3hKhGlUdIlVRtPQJg130_provenance.
• NP324196.RAdw3na8Nd2MrUpz6Z9tocTWhi4qEEQDDtGan-hA2FLrE130_assertion description "[Spinal muscular atrophy (SMA), the leading genetic cause of death in childhood, is an autosomal recessive neuromuscular disorder characterized by progressive muscle weakness, associated with deletions of the survival motor neuron (SMN) gene identified and mapped to chromosome 5q13.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP324196.RAdw3na8Nd2MrUpz6Z9tocTWhi4qEEQDDtGan-hA2FLrE130_provenance.
• NP599771.RAQrXo_bcFKQ6VuGCQ4dZ7Xj7bN7PPz2qTZHDfjNqUGek130_assertion description "[Spinal muscular atrophy (SMA), the leading genetic cause of death in childhood, is an autosomal recessive neuromuscular disorder characterized by progressive muscle weakness, associated with deletions of the survival motor neuron (SMN) gene identified and mapped to chromosome 5q13.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP599771.RAQrXo_bcFKQ6VuGCQ4dZ7Xj7bN7PPz2qTZHDfjNqUGek130_provenance.
• NP420166.RAgIgUpyxN22akBVXUO-xVDjJ2OVqsoFC-OmlD3zjh5J8130_assertion description "[Spinal muscular atrophy (SMA), the leading genetic cause of death in childhood, is an autosomal recessive neuromuscular disorder characterized by progressive muscle weakness, associated with deletions of the survival motor neuron (SMN) gene identified and mapped to chromosome 5q13.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP420166.RAgIgUpyxN22akBVXUO-xVDjJ2OVqsoFC-OmlD3zjh5J8130_provenance.
• NP639076.RAg4ZpnKvgkZ4frIOCF1WEY8zADyPxE40RTEdbv6MjYfs130_assertion description "[Spinal muscular atrophy (SMA), the leading genetic cause of death in childhood, is an autosomal recessive neuromuscular disorder characterized by progressive muscle weakness, associated with deletions of the survival motor neuron (SMN) gene identified and mapped to chromosome 5q13.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP639076.RAg4ZpnKvgkZ4frIOCF1WEY8zADyPxE40RTEdbv6MjYfs130_provenance.
• NP603878.RAqK_I9bh1fXSle_HMVhfTVD8L2EdYS6xPFEgu2Zhwwcg130_assertion description "[Spinal muscular atrophy (SMA), the leading genetic cause of death in childhood, is an autosomal recessive neuromuscular disorder characterized by progressive muscle weakness, associated with deletions of the survival motor neuron (SMN) gene identified and mapped to chromosome 5q13.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP603878.RAqK_I9bh1fXSle_HMVhfTVD8L2EdYS6xPFEgu2Zhwwcg130_provenance.
• NP787000.RATSlJfjcoi9yFb9XFnCVMCP4QSphfretJYnIOe9qfhkg130_assertion description "[Spinal muscular atrophy (SMA), the leading genetic cause of death in childhood, is an autosomal recessive neuromuscular disorder characterized by progressive muscle weakness, associated with deletions of the survival motor neuron (SMN) gene identified and mapped to chromosome 5q13.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP787000.RATSlJfjcoi9yFb9XFnCVMCP4QSphfretJYnIOe9qfhkg130_provenance.
• NP297516.RA-kWArgZ-nH1Fy3sc1-qNPlWfO-GgPF927nLWE4O9bbo130_assertion description "[Spinal muscular atrophy (SMA), the leading genetic cause of death in childhood, is an autosomal recessive neuromuscular disorder characterized by progressive muscle weakness, associated with deletions of the survival motor neuron (SMN) gene identified and mapped to chromosome 5q13.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP297516.RA-kWArgZ-nH1Fy3sc1-qNPlWfO-GgPF927nLWE4O9bbo130_provenance.
• NP531829.RAdnGHSGn23vBIYWN7XC5oN2UO7uYK6kcSRmGIumx3G14130_assertion description "[Spinal muscular atrophy (SMA), the leading genetic cause of death in childhood, is an autosomal recessive neuromuscular disorder characterized by progressive muscle weakness, associated with deletions of the survival motor neuron (SMN) gene identified and mapped to chromosome 5q13.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP531829.RAdnGHSGn23vBIYWN7XC5oN2UO7uYK6kcSRmGIumx3G14130_provenance.
• NP651020.RA_kIF-xVP3ditOiJX7hzV5D4j0CC9tyhP07Aov0XsuE4130_assertion description "[Spinal muscular atrophy (SMA), the leading genetic cause of death in childhood, is an autosomal recessive neuromuscular disorder characterized by progressive muscle weakness, associated with deletions of the survival motor neuron (SMN) gene identified and mapped to chromosome 5q13.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP651020.RA_kIF-xVP3ditOiJX7hzV5D4j0CC9tyhP07Aov0XsuE4130_provenance.
• NP755748.RAzhhYtDUHszHj2QzVnHGZI0wV-NWfdPYd-KrUVj265UQ130_assertion description "[Spinal muscular atrophy (SMA), the leading genetic cause of death in childhood, is an autosomal recessive neuromuscular disorder characterized by progressive muscle weakness, associated with deletions of the survival motor neuron (SMN) gene identified and mapped to chromosome 5q13.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP755748.RAzhhYtDUHszHj2QzVnHGZI0wV-NWfdPYd-KrUVj265UQ130_provenance.
• NP815679.RA5jHx9B5--t_GIGQU-ylykO-F3mbohQBcfwFhN5XXgWs130_assertion description "[Spinal muscular atrophy (SMA), the leading genetic cause of death in childhood, is an autosomal recessive neuromuscular disorder characterized by progressive muscle weakness, associated with deletions of the survival motor neuron (SMN) gene identified and mapped to chromosome 5q13.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP815679.RA5jHx9B5--t_GIGQU-ylykO-F3mbohQBcfwFhN5XXgWs130_provenance.
• NP703548.RAbTl4rIkSZ-p-BFub1Kz4o8xpuHZhLsOlSMXRgED-ILU130_assertion description "[Spinal muscular atrophy (SMA), the leading genetic cause of death in childhood, is an autosomal recessive neuromuscular disorder characterized by progressive muscle weakness, associated with deletions of the survival motor neuron (SMN) gene identified and mapped to chromosome 5q13.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP703548.RAbTl4rIkSZ-p-BFub1Kz4o8xpuHZhLsOlSMXRgED-ILU130_provenance.
• NP705618.RAQazKpsEjVcXpS-pWEKo-i23VMlT9kRrFWu4YpCfGTAQ130_assertion description "[Spinal muscular atrophy (SMA), the leading genetic cause of death in childhood, is an autosomal recessive neuromuscular disorder characterized by progressive muscle weakness, associated with deletions of the survival motor neuron (SMN) gene identified and mapped to chromosome 5q13.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP705618.RAQazKpsEjVcXpS-pWEKo-i23VMlT9kRrFWu4YpCfGTAQ130_provenance.
• NP705631.RAaIeq8weeAorUdiPqmUHa0CC2aGvxq_y1R6Dc5uZUJaE130_assertion description "[Spinal muscular atrophy (SMA), the leading genetic cause of death in childhood, is an autosomal recessive neuromuscular disorder characterized by progressive muscle weakness, associated with deletions of the survival motor neuron (SMN) gene identified and mapped to chromosome 5q13.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP705631.RAaIeq8weeAorUdiPqmUHa0CC2aGvxq_y1R6Dc5uZUJaE130_provenance.
• NP705672.RAb7_3YXFTQpKdjDmxLqcx2GIDNP3gUtbtt404_mF1ZRE130_assertion description "[Spinal muscular atrophy (SMA), the leading genetic cause of death in childhood, is an autosomal recessive neuromuscular disorder characterized by progressive muscle weakness, associated with deletions of the survival motor neuron (SMN) gene identified and mapped to chromosome 5q13.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP705672.RAb7_3YXFTQpKdjDmxLqcx2GIDNP3gUtbtt404_mF1ZRE130_provenance.
• assertion description "[Spinal muscular atrophy (SMA), the leading genetic cause of death in childhood, is an autosomal recessive neuromuscular disorder characterized by progressive muscle weakness, associated with deletions of the survival motor neuron (SMN) gene identified and mapped to chromosome 5q13.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
• NP733320.RAY6AipuTzvtSNSrUCA99KYoBemY7724VJpD2fHPCyUPk130_assertion description "[Spinal muscular atrophy (SMA), the leading genetic cause of death in childhood, is an autosomal recessive neuromuscular disorder characterized by progressive muscle weakness, associated with deletions of the survival motor neuron (SMN) gene identified and mapped to chromosome 5q13.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP733320.RAY6AipuTzvtSNSrUCA99KYoBemY7724VJpD2fHPCyUPk130_provenance.
• NP733324.RAfpIuSeFBZTbmLxKyxPKqA3hAISQyyJpyQW1r2xfOpNs130_assertion description "[Spinal muscular atrophy (SMA), the leading genetic cause of death in childhood, is an autosomal recessive neuromuscular disorder characterized by progressive muscle weakness, associated with deletions of the survival motor neuron (SMN) gene identified and mapped to chromosome 5q13.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP733324.RAfpIuSeFBZTbmLxKyxPKqA3hAISQyyJpyQW1r2xfOpNs130_provenance.
• NP531785.RABwI3MW0LV2x7pI3ExM1w-9f3227FpGjaE7CEhSifaxo130_assertion description "[Spinal muscular atrophy (SMA), the leading genetic cause of death in childhood, is an autosomal recessive neuromuscular disorder characterized by progressive muscle weakness, associated with deletions of the survival motor neuron (SMN) gene identified and mapped to chromosome 5q13.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP531785.RABwI3MW0LV2x7pI3ExM1w-9f3227FpGjaE7CEhSifaxo130_provenance.
• NP733328.RABh1mRzPOUhBFu-L4Z--9p4KPbNLIlNYZf8EKIS-K-5c130_assertion description "[Spinal muscular atrophy (SMA), the leading genetic cause of death in childhood, is an autosomal recessive neuromuscular disorder characterized by progressive muscle weakness, associated with deletions of the survival motor neuron (SMN) gene identified and mapped to chromosome 5q13.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP733328.RABh1mRzPOUhBFu-L4Z--9p4KPbNLIlNYZf8EKIS-K-5c130_provenance.
• NP733318.RAnr5LUIZ8Sehh5g7QTCiwQ6BEKC3GLWMwGg9knI-h0kk130_assertion description "[Spinal muscular atrophy (SMA), the leading genetic cause of death in childhood, is an autosomal recessive neuromuscular disorder characterized by progressive muscle weakness, associated with deletions of the survival motor neuron (SMN) gene identified and mapped to chromosome 5q13.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP733318.RAnr5LUIZ8Sehh5g7QTCiwQ6BEKC3GLWMwGg9knI-h0kk130_provenance.
• NP733319.RAjBQitM3wfeL2z8PgtJOsAHPsgkJCW2rjvN0m8skixlc130_assertion description "[Spinal muscular atrophy (SMA), the leading genetic cause of death in childhood, is an autosomal recessive neuromuscular disorder characterized by progressive muscle weakness, associated with deletions of the survival motor neuron (SMN) gene identified and mapped to chromosome 5q13.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP733319.RAjBQitM3wfeL2z8PgtJOsAHPsgkJCW2rjvN0m8skixlc130_provenance.
• NP531767.RAE91gqKvdwSUdOnQFXN59J9UdkwtrzUxHBR1XsdbzkgQ130_assertion description "[Spinal muscular atrophy (SMA), the leading genetic cause of death in childhood, is an autosomal recessive neuromuscular disorder characterized by progressive muscle weakness, associated with deletions of the survival motor neuron (SMN) gene identified and mapped to chromosome 5q13.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP531767.RAE91gqKvdwSUdOnQFXN59J9UdkwtrzUxHBR1XsdbzkgQ130_provenance.
• NP703501.RAGTHUHdubbc9mEJSuDfj0ntzlYrG2A-hs0w_JDqwLnI0130_assertion description "[Spinal muscular atrophy (SMA), the leading genetic cause of death in childhood, is an autosomal recessive neuromuscular disorder characterized by progressive muscle weakness, associated with deletions of the survival motor neuron (SMN) gene identified and mapped to chromosome 5q13.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP703501.RAGTHUHdubbc9mEJSuDfj0ntzlYrG2A-hs0w_JDqwLnI0130_provenance.
• NP703870.RAFE-9c_BofHDchI3RU1fmRKKEzT0RUoAGCfWaj--BF70130_assertion description "[Spinal muscular atrophy (SMA), the leading genetic cause of death in childhood, is an autosomal recessive neuromuscular disorder characterized by progressive muscle weakness, associated with deletions of the survival motor neuron (SMN) gene identified and mapped to chromosome 5q13.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP703870.RAFE-9c_BofHDchI3RU1fmRKKEzT0RUoAGCfWaj--BF70130_provenance.
• NP733321.RALevzME5yUrCtou7G0QGTLIcWegmZlKTmt9y_b1to_Wk130_assertion description "[Spinal muscular atrophy (SMA), the leading genetic cause of death in childhood, is an autosomal recessive neuromuscular disorder characterized by progressive muscle weakness, associated with deletions of the survival motor neuron (SMN) gene identified and mapped to chromosome 5q13.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP733321.RALevzME5yUrCtou7G0QGTLIcWegmZlKTmt9y_b1to_Wk130_provenance.
• NP733322.RAP_DDre8GSXlPfT1FLWaBwpr0_myYUqboVIvMWBGoqz4130_assertion description "[Spinal muscular atrophy (SMA), the leading genetic cause of death in childhood, is an autosomal recessive neuromuscular disorder characterized by progressive muscle weakness, associated with deletions of the survival motor neuron (SMN) gene identified and mapped to chromosome 5q13.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP733322.RAP_DDre8GSXlPfT1FLWaBwpr0_myYUqboVIvMWBGoqz4130_provenance.
• NP733325.RAN0BgDuNWAtyIdGqD-EPdD0_kJ9cxDIL1vZIjEYnMIcg130_assertion description "[Spinal muscular atrophy (SMA), the leading genetic cause of death in childhood, is an autosomal recessive neuromuscular disorder characterized by progressive muscle weakness, associated with deletions of the survival motor neuron (SMN) gene identified and mapped to chromosome 5q13.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP733325.RAN0BgDuNWAtyIdGqD-EPdD0_kJ9cxDIL1vZIjEYnMIcg130_provenance.
• NP733327.RAGm3togck7zAS4MIl1BC6iYz0KDlEdSl7oGtcUpsKXRw130_assertion description "[Spinal muscular atrophy (SMA), the leading genetic cause of death in childhood, is an autosomal recessive neuromuscular disorder characterized by progressive muscle weakness, associated with deletions of the survival motor neuron (SMN) gene identified and mapped to chromosome 5q13.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP733327.RAGm3togck7zAS4MIl1BC6iYz0KDlEdSl7oGtcUpsKXRw130_provenance.
• NP733330.RAGSRo256QOFHeHUIlWJAWvZpjoCemspo8A7dVyHnciX4130_assertion description "[Spinal muscular atrophy (SMA), the leading genetic cause of death in childhood, is an autosomal recessive neuromuscular disorder characterized by progressive muscle weakness, associated with deletions of the survival motor neuron (SMN) gene identified and mapped to chromosome 5q13.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP733330.RAGSRo256QOFHeHUIlWJAWvZpjoCemspo8A7dVyHnciX4130_provenance.
• NP733331.RANm68zkEsgnNiDQiuM-YaFANpHi2YU9kvvU_GKN5PPrU130_assertion description "[Spinal muscular atrophy (SMA), the leading genetic cause of death in childhood, is an autosomal recessive neuromuscular disorder characterized by progressive muscle weakness, associated with deletions of the survival motor neuron (SMN) gene identified and mapped to chromosome 5q13.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP733331.RANm68zkEsgnNiDQiuM-YaFANpHi2YU9kvvU_GKN5PPrU130_provenance.
• NP703823.RAx1eiu2rpHhAhQUEuRxcxZAeMERJOjGa_Y36YEW9C49U130_assertion description "[Spinal muscular atrophy (SMA), the leading genetic cause of death in childhood, is an autosomal recessive neuromuscular disorder characterized by progressive muscle weakness, associated with deletions of the survival motor neuron (SMN) gene identified and mapped to chromosome 5q13.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP703823.RAx1eiu2rpHhAhQUEuRxcxZAeMERJOjGa_Y36YEW9C49U130_provenance.
• NP733317.RA0DemV6FP5N5jZFhGaiPvJJByoJJfWepxgJdrS1LaEJQ130_assertion description "[Spinal muscular atrophy (SMA), the leading genetic cause of death in childhood, is an autosomal recessive neuromuscular disorder characterized by progressive muscle weakness, associated with deletions of the survival motor neuron (SMN) gene identified and mapped to chromosome 5q13.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP733317.RA0DemV6FP5N5jZFhGaiPvJJByoJJfWepxgJdrS1LaEJQ130_provenance.
• NP733323.RA4HeexYDqv6uaO-SlH-_Esb2vjYUOriH1Zjw6Kjr8Cp4130_assertion description "[Spinal muscular atrophy (SMA), the leading genetic cause of death in childhood, is an autosomal recessive neuromuscular disorder characterized by progressive muscle weakness, associated with deletions of the survival motor neuron (SMN) gene identified and mapped to chromosome 5q13.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP733323.RA4HeexYDqv6uaO-SlH-_Esb2vjYUOriH1Zjw6Kjr8Cp4130_provenance.
• NP733326.RAwomBJUTQRFo4WP02tYBuUjpsyOwRUYDTc3uyKvNbanE130_assertion description "[Spinal muscular atrophy (SMA), the leading genetic cause of death in childhood, is an autosomal recessive neuromuscular disorder characterized by progressive muscle weakness, associated with deletions of the survival motor neuron (SMN) gene identified and mapped to chromosome 5q13.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP733326.RAwomBJUTQRFo4WP02tYBuUjpsyOwRUYDTc3uyKvNbanE130_provenance.