Nanopublications LDF server

Matches in Nanopublications for { ?s ?p "[FMR1 is an RNA-binding protein that is either absent or mutated in patients affected by the fragile X syndrome, the most common inherited cause of mental retardation in humans.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ?g. }

• NP156451.RABD2XojMY_dyKJDuuH_vP06Q5Gp-8j2znIVvpalPljEs130_assertion description "[FMR1 is an RNA-binding protein that is either absent or mutated in patients affected by the fragile X syndrome, the most common inherited cause of mental retardation in humans.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP156451.RABD2XojMY_dyKJDuuH_vP06Q5Gp-8j2znIVvpalPljEs130_provenance.
• NP765200.RAhOIKi-OmhLnaffchx1T3m9-iEGUHP6DWaJKVI14_GvY130_assertion description "[FMR1 is an RNA-binding protein that is either absent or mutated in patients affected by the fragile X syndrome, the most common inherited cause of mental retardation in humans.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP765200.RAhOIKi-OmhLnaffchx1T3m9-iEGUHP6DWaJKVI14_GvY130_provenance.
• NP330996.RAdE3NlPH8DeXdcAXhMPv3oCOsK52Eg6jWhPJ7dRpVh_c130_assertion description "[FMR1 is an RNA-binding protein that is either absent or mutated in patients affected by the fragile X syndrome, the most common inherited cause of mental retardation in humans.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP330996.RAdE3NlPH8DeXdcAXhMPv3oCOsK52Eg6jWhPJ7dRpVh_c130_provenance.
• NP883314.RAsARHK8YmP-RSAagHTkVfevey6IgzGRgvWoTUnazkOwQ130_assertion description "[FMR1 is an RNA-binding protein that is either absent or mutated in patients affected by the fragile X syndrome, the most common inherited cause of mental retardation in humans.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP883314.RAsARHK8YmP-RSAagHTkVfevey6IgzGRgvWoTUnazkOwQ130_provenance.
• NP490657.RADdXXQFmFxfx6LUkng3n6erVjB54cxZOyzOgw3FLrQIM130_assertion description "[FMR1 is an RNA-binding protein that is either absent or mutated in patients affected by the fragile X syndrome, the most common inherited cause of mental retardation in humans.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP490657.RADdXXQFmFxfx6LUkng3n6erVjB54cxZOyzOgw3FLrQIM130_provenance.
• NP518827.RAmdsWzH1Ik950dQpyVLvctNbB4so5L8kbTJK3XJMLniI130_assertion description "[FMR1 is an RNA-binding protein that is either absent or mutated in patients affected by the fragile X syndrome, the most common inherited cause of mental retardation in humans.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP518827.RAmdsWzH1Ik950dQpyVLvctNbB4so5L8kbTJK3XJMLniI130_provenance.
• NP495853.RAiyclpO4UaxirPTR4u-6bdGT35-DjoSCCsH-5vp4vFh8130_assertion description "[FMR1 is an RNA-binding protein that is either absent or mutated in patients affected by the fragile X syndrome, the most common inherited cause of mental retardation in humans.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP495853.RAiyclpO4UaxirPTR4u-6bdGT35-DjoSCCsH-5vp4vFh8130_provenance.
• NP915982.RAr_QN0BsRXcEmZ-6wsFk8r9S99LVkt2fd7OhVfnaGSgI130_assertion description "[FMR1 is an RNA-binding protein that is either absent or mutated in patients affected by the fragile X syndrome, the most common inherited cause of mental retardation in humans.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP915982.RAr_QN0BsRXcEmZ-6wsFk8r9S99LVkt2fd7OhVfnaGSgI130_provenance.
• assertion description "[FMR1 is an RNA-binding protein that is either absent or mutated in patients affected by the fragile X syndrome, the most common inherited cause of mental retardation in humans.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
• assertion description "[FMR1 is an RNA-binding protein that is either absent or mutated in patients affected by the fragile X syndrome, the most common inherited cause of mental retardation in humans.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
• NP236650.RA_CqJAPV_6-hXo0tff8YFfDDVCz4yL96pWDfKJG7HEuQ130_assertion description "[FMR1 is an RNA-binding protein that is either absent or mutated in patients affected by the fragile X syndrome, the most common inherited cause of mental retardation in humans.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP236650.RA_CqJAPV_6-hXo0tff8YFfDDVCz4yL96pWDfKJG7HEuQ130_provenance.
• NP295980.RAMKk6acwVtfW0_jx0IKmlhPIj85ezuj8PRLdCDrulhNE130_assertion description "[FMR1 is an RNA-binding protein that is either absent or mutated in patients affected by the fragile X syndrome, the most common inherited cause of mental retardation in humans.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP295980.RAMKk6acwVtfW0_jx0IKmlhPIj85ezuj8PRLdCDrulhNE130_provenance.
• NP874255.RAVT27NfEm5xBtjg32I1qwJ8xm9aQg3An2O3yCXlRCLoM130_assertion description "[FMR1 is an RNA-binding protein that is either absent or mutated in patients affected by the fragile X syndrome, the most common inherited cause of mental retardation in humans.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP874255.RAVT27NfEm5xBtjg32I1qwJ8xm9aQg3An2O3yCXlRCLoM130_provenance.
• NP874291.RATUcL2iYWwsFhSAyg7cceMAnS9qGSGoeRJ7kJEUKrZgU130_assertion description "[FMR1 is an RNA-binding protein that is either absent or mutated in patients affected by the fragile X syndrome, the most common inherited cause of mental retardation in humans.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP874291.RATUcL2iYWwsFhSAyg7cceMAnS9qGSGoeRJ7kJEUKrZgU130_provenance.
• NP887916.RAVj4PqS4nee5pPmkd6Ant5NydIF1qBnIxu2_LqmE116c130_assertion description "[FMR1 is an RNA-binding protein that is either absent or mutated in patients affected by the fragile X syndrome, the most common inherited cause of mental retardation in humans.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP887916.RAVj4PqS4nee5pPmkd6Ant5NydIF1qBnIxu2_LqmE116c130_provenance.
• NP551493.RAIy_UsQwTwRbYfovURFwrAJ8uDcEZNhZSlCkiGyRK_ok130_assertion description "[FMR1 is an RNA-binding protein that is either absent or mutated in patients affected by the fragile X syndrome, the most common inherited cause of mental retardation in humans.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP551493.RAIy_UsQwTwRbYfovURFwrAJ8uDcEZNhZSlCkiGyRK_ok130_provenance.
• NP924500.RAUVUP-2J8bud_zB-daRlN_t_uDSevGF3l1pzeyzu0sB8130_assertion description "[FMR1 is an RNA-binding protein that is either absent or mutated in patients affected by the fragile X syndrome, the most common inherited cause of mental retardation in humans.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP924500.RAUVUP-2J8bud_zB-daRlN_t_uDSevGF3l1pzeyzu0sB8130_provenance.
• NP924536.RAeGcYlbsxxnNSIeFbv9fj1F5b9rvKT09TSbcChqoHWPE130_assertion description "[FMR1 is an RNA-binding protein that is either absent or mutated in patients affected by the fragile X syndrome, the most common inherited cause of mental retardation in humans.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP924536.RAeGcYlbsxxnNSIeFbv9fj1F5b9rvKT09TSbcChqoHWPE130_provenance.
• NP576461.RAOedvgNNWOpmbhAubnEAGTwkS5fOJhL7JeHKWhcFj-5Y130_assertion description "[FMR1 is an RNA-binding protein that is either absent or mutated in patients affected by the fragile X syndrome, the most common inherited cause of mental retardation in humans.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP576461.RAOedvgNNWOpmbhAubnEAGTwkS5fOJhL7JeHKWhcFj-5Y130_provenance.
• assertion description "[FMR1 is an RNA-binding protein that is either absent or mutated in patients affected by the fragile X syndrome, the most common inherited cause of mental retardation in humans.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
• assertion description "[FMR1 is an RNA-binding protein that is either absent or mutated in patients affected by the fragile X syndrome, the most common inherited cause of mental retardation in humans.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
• assertion description "[FMR1 is an RNA-binding protein that is either absent or mutated in patients affected by the fragile X syndrome, the most common inherited cause of mental retardation in humans.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
• assertion description "[FMR1 is an RNA-binding protein that is either absent or mutated in patients affected by the fragile X syndrome, the most common inherited cause of mental retardation in humans.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
• assertion description "[FMR1 is an RNA-binding protein that is either absent or mutated in patients affected by the fragile X syndrome, the most common inherited cause of mental retardation in humans.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
• assertion description "[FMR1 is an RNA-binding protein that is either absent or mutated in patients affected by the fragile X syndrome, the most common inherited cause of mental retardation in humans.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
• assertion description "[FMR1 is an RNA-binding protein that is either absent or mutated in patients affected by the fragile X syndrome, the most common inherited cause of mental retardation in humans.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
• assertion description "[FMR1 is an RNA-binding protein that is either absent or mutated in patients affected by the fragile X syndrome, the most common inherited cause of mental retardation in humans.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
• assertion description "[FMR1 is an RNA-binding protein that is either absent or mutated in patients affected by the fragile X syndrome, the most common inherited cause of mental retardation in humans.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
• assertion description "[FMR1 is an RNA-binding protein that is either absent or mutated in patients affected by the fragile X syndrome, the most common inherited cause of mental retardation in humans.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
• assertion description "[FMR1 is an RNA-binding protein that is either absent or mutated in patients affected by the fragile X syndrome, the most common inherited cause of mental retardation in humans.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
• assertion description "[FMR1 is an RNA-binding protein that is either absent or mutated in patients affected by the fragile X syndrome, the most common inherited cause of mental retardation in humans.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
• NP263785.RAaPchshyGCe1M19u8URQePM0P8HIzRnLMGOE9jsA4j-A130_assertion description "[FMR1 is an RNA-binding protein that is either absent or mutated in patients affected by the fragile X syndrome, the most common inherited cause of mental retardation in humans.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP263785.RAaPchshyGCe1M19u8URQePM0P8HIzRnLMGOE9jsA4j-A130_provenance.
• NP263790.RAUyssdWnba7QW0xrVqENFEEU4LQkdPU_zIHh3rhu5HB8130_assertion description "[FMR1 is an RNA-binding protein that is either absent or mutated in patients affected by the fragile X syndrome, the most common inherited cause of mental retardation in humans.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP263790.RAUyssdWnba7QW0xrVqENFEEU4LQkdPU_zIHh3rhu5HB8130_provenance.
• NP263794.RAU9OIt0JbqPtwx1afMBGB0fHDdUUGxrZ-C1GBo-48zDg130_assertion description "[FMR1 is an RNA-binding protein that is either absent or mutated in patients affected by the fragile X syndrome, the most common inherited cause of mental retardation in humans.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP263794.RAU9OIt0JbqPtwx1afMBGB0fHDdUUGxrZ-C1GBo-48zDg130_provenance.
• NP263796.RARGb99aZ913J3sNYZzdRxmcEdbFC9SLYg1_PYe-2cYoY130_assertion description "[FMR1 is an RNA-binding protein that is either absent or mutated in patients affected by the fragile X syndrome, the most common inherited cause of mental retardation in humans.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP263796.RARGb99aZ913J3sNYZzdRxmcEdbFC9SLYg1_PYe-2cYoY130_provenance.
• NP652754.RACD0fyUuuA5PdRuAn1BCNobpAKUwiaX3tq-AyDCKBrCQ130_assertion description "[FMR1 is an RNA-binding protein that is either absent or mutated in patients affected by the fragile X syndrome, the most common inherited cause of mental retardation in humans.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP652754.RACD0fyUuuA5PdRuAn1BCNobpAKUwiaX3tq-AyDCKBrCQ130_provenance.
• assertion description "[FMR1 is an RNA-binding protein that is either absent or mutated in patients affected by the fragile X syndrome, the most common inherited cause of mental retardation in humans.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
• assertion description "[FMR1 is an RNA-binding protein that is either absent or mutated in patients affected by the fragile X syndrome, the most common inherited cause of mental retardation in humans.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
• assertion description "[FMR1 is an RNA-binding protein that is either absent or mutated in patients affected by the fragile X syndrome, the most common inherited cause of mental retardation in humans.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
• NP667799.RAieY5RAVO8tMY_h_Ku6JWOijidhWRE1HCh63Ph2dTTqI130_assertion description "[FMR1 is an RNA-binding protein that is either absent or mutated in patients affected by the fragile X syndrome, the most common inherited cause of mental retardation in humans.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP667799.RAieY5RAVO8tMY_h_Ku6JWOijidhWRE1HCh63Ph2dTTqI130_provenance.
• NP263784.RAsZHfuKzJ4_M07KzWbviiTz3maqYsthAobpuVbcHtins130_assertion description "[FMR1 is an RNA-binding protein that is either absent or mutated in patients affected by the fragile X syndrome, the most common inherited cause of mental retardation in humans.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP263784.RAsZHfuKzJ4_M07KzWbviiTz3maqYsthAobpuVbcHtins130_provenance.
• NP263795.RAih6W83w2Omvcz_ipwqOoJuhbVgOc_W8RTbX0d9quweg130_assertion description "[FMR1 is an RNA-binding protein that is either absent or mutated in patients affected by the fragile X syndrome, the most common inherited cause of mental retardation in humans.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP263795.RAih6W83w2Omvcz_ipwqOoJuhbVgOc_W8RTbX0d9quweg130_provenance.
• NP887952.RAqkOpFa3dSTE0Qsr0UwbzPmTWoDQZJPklW7Daanxn3h4130_assertion description "[FMR1 is an RNA-binding protein that is either absent or mutated in patients affected by the fragile X syndrome, the most common inherited cause of mental retardation in humans.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP887952.RAqkOpFa3dSTE0Qsr0UwbzPmTWoDQZJPklW7Daanxn3h4130_provenance.
• NP956616.RAugjM6H4jIKOlGdNceWemFCExTelww4krCrX8JiNDIdE130_assertion description "[FMR1 is an RNA-binding protein that is either absent or mutated in patients affected by the fragile X syndrome, the most common inherited cause of mental retardation in humans.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP956616.RAugjM6H4jIKOlGdNceWemFCExTelww4krCrX8JiNDIdE130_provenance.
• NP956652.RAslpC1ybcA2CFPfdHPpPVi_vqyrdMJ6RoZpfTzy2gz9Q130_assertion description "[FMR1 is an RNA-binding protein that is either absent or mutated in patients affected by the fragile X syndrome, the most common inherited cause of mental retardation in humans.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP956652.RAslpC1ybcA2CFPfdHPpPVi_vqyrdMJ6RoZpfTzy2gz9Q130_provenance.
• NP667836.RA5X08w4kQsvPIzjeh3SqSE0LEsb13Vn2Hg1d0vExu92A130_assertion description "[FMR1 is an RNA-binding protein that is either absent or mutated in patients affected by the fragile X syndrome, the most common inherited cause of mental retardation in humans.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP667836.RA5X08w4kQsvPIzjeh3SqSE0LEsb13Vn2Hg1d0vExu92A130_provenance.
• NP263788.RAEgNgrwjbfNZEfCdnv9_xOclRu9gSCxsx2rV2oM9YaWY130_assertion description "[FMR1 is an RNA-binding protein that is either absent or mutated in patients affected by the fragile X syndrome, the most common inherited cause of mental retardation in humans.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP263788.RAEgNgrwjbfNZEfCdnv9_xOclRu9gSCxsx2rV2oM9YaWY130_provenance.
• NP263797.RAHrMH-1KXaQ4eaextZsp-x21ExJUp0KHK-KoYw2D-UR4130_assertion description "[FMR1 is an RNA-binding protein that is either absent or mutated in patients affected by the fragile X syndrome, the most common inherited cause of mental retardation in humans.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP263797.RAHrMH-1KXaQ4eaextZsp-x21ExJUp0KHK-KoYw2D-UR4130_provenance.
• NP652709.RAymgGxDmRDJNS4s-rWSYKLGMprpSp0hMr5ubyXK_VLFA130_assertion description "[FMR1 is an RNA-binding protein that is either absent or mutated in patients affected by the fragile X syndrome, the most common inherited cause of mental retardation in humans.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP652709.RAymgGxDmRDJNS4s-rWSYKLGMprpSp0hMr5ubyXK_VLFA130_provenance.
• NP263786.RA0vIct3l3u_u6MBHlj9b2Ic-VmoNWxes5GZ5QWzedHhc130_assertion description "[FMR1 is an RNA-binding protein that is either absent or mutated in patients affected by the fragile X syndrome, the most common inherited cause of mental retardation in humans.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP263786.RA0vIct3l3u_u6MBHlj9b2Ic-VmoNWxes5GZ5QWzedHhc130_provenance.
• NP263787.RAwAcUuWCHdGFnv0IAorKyJw6_QAMzN5qMnLRgtN25whc130_assertion description "[FMR1 is an RNA-binding protein that is either absent or mutated in patients affected by the fragile X syndrome, the most common inherited cause of mental retardation in humans.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP263787.RAwAcUuWCHdGFnv0IAorKyJw6_QAMzN5qMnLRgtN25whc130_provenance.
• NP263789.RA_GuJsU6kRaai-rm_SV-eMfbOxJLVfr3rLcx0Qa4pMbs130_assertion description "[FMR1 is an RNA-binding protein that is either absent or mutated in patients affected by the fragile X syndrome, the most common inherited cause of mental retardation in humans.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP263789.RA_GuJsU6kRaai-rm_SV-eMfbOxJLVfr3rLcx0Qa4pMbs130_provenance.
• NP263791.RAym4YlYb7W7pPX4fho-0jI0HWz20ZplQWQtM4dVZcW7A130_assertion description "[FMR1 is an RNA-binding protein that is either absent or mutated in patients affected by the fragile X syndrome, the most common inherited cause of mental retardation in humans.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP263791.RAym4YlYb7W7pPX4fho-0jI0HWz20ZplQWQtM4dVZcW7A130_provenance.
• NP263792.RA9cIZP8_K-IU76XUl_QlODCSEDRWLJI8ZQasfBGEMPcU130_assertion description "[FMR1 is an RNA-binding protein that is either absent or mutated in patients affected by the fragile X syndrome, the most common inherited cause of mental retardation in humans.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP263792.RA9cIZP8_K-IU76XUl_QlODCSEDRWLJI8ZQasfBGEMPcU130_provenance.
• NP263793.RA3UKYBch5qh5wJHGNckj4R0l0glmA1K5Bhl5PxvWbAHo130_assertion description "[FMR1 is an RNA-binding protein that is either absent or mutated in patients affected by the fragile X syndrome, the most common inherited cause of mental retardation in humans.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP263793.RA3UKYBch5qh5wJHGNckj4R0l0glmA1K5Bhl5PxvWbAHo130_provenance.