Nanopublications LDF server

Matches in Nanopublications for { ?s ?p "[Most cases of Rett syndrome (RTT) are caused by mutations in the methylated DNA-binding protein, MeCP2.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ?g. }

• NP181968.RAU1pmZflz9NhYeej4QIFsFg_g0iqicJIBPY3M0et_8OQ130_assertion description "[Most cases of Rett syndrome (RTT) are caused by mutations in the methylated DNA-binding protein, MeCP2.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP181968.RAU1pmZflz9NhYeej4QIFsFg_g0iqicJIBPY3M0et_8OQ130_provenance.
• NP490377.RAdi61wxDeEuU4RJ4K8yMkQbNntKYhDwdn5vi0cCXezY8130_assertion description "[Most cases of Rett syndrome (RTT) are caused by mutations in the methylated DNA-binding protein, MeCP2.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP490377.RAdi61wxDeEuU4RJ4K8yMkQbNntKYhDwdn5vi0cCXezY8130_provenance.
• NP877720.RAYML4tBWRfyerhlArCApPcADdvD1RU4bBVX_8Y6h3iOs130_assertion description "[Most cases of Rett syndrome (RTT) are caused by mutations in the methylated DNA-binding protein, MeCP2.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP877720.RAYML4tBWRfyerhlArCApPcADdvD1RU4bBVX_8Y6h3iOs130_provenance.
• NP335874.RACAR5-EDiF83-mduL67RkxwODIdO6mhYAg9brAWQI4Gc130_assertion description "[Most cases of Rett syndrome (RTT) are caused by mutations in the methylated DNA-binding protein, MeCP2.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP335874.RACAR5-EDiF83-mduL67RkxwODIdO6mhYAg9brAWQI4Gc130_provenance.
• NP818639.RADyeyywXFUp-vVGgmKPs8CW9oMaxOuljgOTug9X6ROlU130_assertion description "[Most cases of Rett syndrome (RTT) are caused by mutations in the methylated DNA-binding protein, MeCP2.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP818639.RADyeyywXFUp-vVGgmKPs8CW9oMaxOuljgOTug9X6ROlU130_provenance.
• NP523629.RAhJ9zYmMOcW5vO0d3K_B9ZXsIbolw1XnMI3Sk_D-fFAE130_assertion description "[Most cases of Rett syndrome (RTT) are caused by mutations in the methylated DNA-binding protein, MeCP2.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP523629.RAhJ9zYmMOcW5vO0d3K_B9ZXsIbolw1XnMI3Sk_D-fFAE130_provenance.
• NP297726.RAc_tr6-woy0-Jhh8-b6JDWSKV0SthDVXAUiGtDvt2s4E130_assertion description "[Most cases of Rett syndrome (RTT) are caused by mutations in the methylated DNA-binding protein, MeCP2.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP297726.RAc_tr6-woy0-Jhh8-b6JDWSKV0SthDVXAUiGtDvt2s4E130_provenance.
• NP196954.RAH6YUcKXlOtYRCS1Dvc7euu1lsNHDlWyxR2xOv9zpZ9E130_assertion description "[Most cases of Rett syndrome (RTT) are caused by mutations in the methylated DNA-binding protein, MeCP2.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP196954.RAH6YUcKXlOtYRCS1Dvc7euu1lsNHDlWyxR2xOv9zpZ9E130_provenance.
• NP739657.RA2hIufZ6JSObEXzSpBB58Au0JYwEccUUqIVBzUe3cgKI130_assertion description "[Most cases of Rett syndrome (RTT) are caused by mutations in the methylated DNA-binding protein, MeCP2.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP739657.RA2hIufZ6JSObEXzSpBB58Au0JYwEccUUqIVBzUe3cgKI130_provenance.
• NP871124.RAD0pbOW8ys8g1FE-439p2-exLDp1H82E-Ms1EPV0-3k4130_assertion description "[Most cases of Rett syndrome (RTT) are caused by mutations in the methylated DNA-binding protein, MeCP2.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP871124.RAD0pbOW8ys8g1FE-439p2-exLDp1H82E-Ms1EPV0-3k4130_provenance.
• NP989222.RADCUIo7pUc4yUB7zPb-PnQt8-PyEXaU-GOcDq37QCTOk130_assertion description "[Most cases of Rett syndrome (RTT) are caused by mutations in the methylated DNA-binding protein, MeCP2.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP989222.RADCUIo7pUc4yUB7zPb-PnQt8-PyEXaU-GOcDq37QCTOk130_provenance.
• NP417811.RA-t6FZ13mRN-3sSCHqqGc7nkQNaDmIWbkgB8craYjIHY130_assertion description "[Most cases of Rett syndrome (RTT) are caused by mutations in the methylated DNA-binding protein, MeCP2.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP417811.RA-t6FZ13mRN-3sSCHqqGc7nkQNaDmIWbkgB8craYjIHY130_provenance.
• NP676359.RAzs7pbZyRZWC_0D-DJ5EEBPn18V0y3tB_YDrnNpw6v3E130_assertion description "[Most cases of Rett syndrome (RTT) are caused by mutations in the methylated DNA-binding protein, MeCP2.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP676359.RAzs7pbZyRZWC_0D-DJ5EEBPn18V0y3tB_YDrnNpw6v3E130_provenance.
• NP764898.RAx2JjduzTRHI6Sm4Wuhg2i-4orkU1pk4VipAJloSKt5A130_assertion description "[Most cases of Rett syndrome (RTT) are caused by mutations in the methylated DNA-binding protein, MeCP2.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP764898.RAx2JjduzTRHI6Sm4Wuhg2i-4orkU1pk4VipAJloSKt5A130_provenance.
• assertion description "[Most cases of Rett syndrome (RTT) are caused by mutations in the methylated DNA-binding protein, MeCP2.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
• NP975045.RA68NSBZHnNzFV5qX1JF1lKkhbM40ScYIFfu7hUm6ZiXo130_assertion description "[Most cases of Rett syndrome (RTT) are caused by mutations in the methylated DNA-binding protein, MeCP2.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP975045.RA68NSBZHnNzFV5qX1JF1lKkhbM40ScYIFfu7hUm6ZiXo130_provenance.
• NP984218.RA7h-dH24Z0OPEa9Wvi_VcLLtxo8xpEXbJUIt4Jje3g6Y130_assertion description "[Most cases of Rett syndrome (RTT) are caused by mutations in the methylated DNA-binding protein, MeCP2.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP984218.RA7h-dH24Z0OPEa9Wvi_VcLLtxo8xpEXbJUIt4Jje3g6Y130_provenance.
• NP672829.RA-uW0DL8ELnsy0OKRR8aJ8vYPZD1JyUUKKK1Gd6f70cw130_assertion description "[Most cases of Rett syndrome (RTT) are caused by mutations in the methylated DNA-binding protein, MeCP2.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP672829.RA-uW0DL8ELnsy0OKRR8aJ8vYPZD1JyUUKKK1Gd6f70cw130_provenance.
• NP672830.RAz_bYstp7o0AkJBf2AX08SJ2MBw9JDXcZlO775MToR7c130_assertion description "[Most cases of Rett syndrome (RTT) are caused by mutations in the methylated DNA-binding protein, MeCP2.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP672830.RAz_bYstp7o0AkJBf2AX08SJ2MBw9JDXcZlO775MToR7c130_provenance.
• NP672824.RAYFsL4nCQmRnBwyTgrD41Finblnfu_HX2Y6RlPTgQr34130_assertion description "[Most cases of Rett syndrome (RTT) are caused by mutations in the methylated DNA-binding protein, MeCP2.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP672824.RAYFsL4nCQmRnBwyTgrD41Finblnfu_HX2Y6RlPTgQr34130_provenance.
• NP672825.RAfTrPfXDqadOaAF03WaYApSq2b-2tOlVToNJoVZrPXpc130_assertion description "[Most cases of Rett syndrome (RTT) are caused by mutations in the methylated DNA-binding protein, MeCP2.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP672825.RAfTrPfXDqadOaAF03WaYApSq2b-2tOlVToNJoVZrPXpc130_provenance.
• assertion description "[Most cases of Rett syndrome (RTT) are caused by mutations in the methylated DNA-binding protein, MeCP2.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
• assertion description "[Most cases of Rett syndrome (RTT) are caused by mutations in the methylated DNA-binding protein, MeCP2.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
• assertion description "[Most cases of Rett syndrome (RTT) are caused by mutations in the methylated DNA-binding protein, MeCP2.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
• assertion description "[Most cases of Rett syndrome (RTT) are caused by mutations in the methylated DNA-binding protein, MeCP2.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
• assertion description "[Most cases of Rett syndrome (RTT) are caused by mutations in the methylated DNA-binding protein, MeCP2.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
• assertion description "[Most cases of Rett syndrome (RTT) are caused by mutations in the methylated DNA-binding protein, MeCP2.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
• assertion description "[Most cases of Rett syndrome (RTT) are caused by mutations in the methylated DNA-binding protein, MeCP2.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
• NP989292.RAk7BKfAVMCE1nJLoA1yDNZTYJZKK0yxzRS-89qMw-AB8130_assertion description "[Most cases of Rett syndrome (RTT) are caused by mutations in the methylated DNA-binding protein, MeCP2.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP989292.RAk7BKfAVMCE1nJLoA1yDNZTYJZKK0yxzRS-89qMw-AB8130_provenance.
• assertion description "[Most cases of Rett syndrome (RTT) are caused by mutations in the methylated DNA-binding protein, MeCP2.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
• assertion description "[Most cases of Rett syndrome (RTT) are caused by mutations in the methylated DNA-binding protein, MeCP2.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
• NP922894.RAOIXfDQgTMCSlTfmR2UwzsDme9_xNOmuzHVJ3WM2sBgE130_assertion description "[Most cases of Rett syndrome (RTT) are caused by mutations in the methylated DNA-binding protein, MeCP2.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP922894.RAOIXfDQgTMCSlTfmR2UwzsDme9_xNOmuzHVJ3WM2sBgE130_provenance.
• NP428521.RAtFHq9s26YvG2S0NWSdPHP_BakX7RcmvSevmQMVsa1Do130_assertion description "[Most cases of Rett syndrome (RTT) are caused by mutations in the methylated DNA-binding protein, MeCP2.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP428521.RAtFHq9s26YvG2S0NWSdPHP_BakX7RcmvSevmQMVsa1Do130_provenance.
• NP672827.RAI5CSe7WmzzGaH2319SRLSOSsWjgnX-aPrQfHtpgzT9U130_assertion description "[Most cases of Rett syndrome (RTT) are caused by mutations in the methylated DNA-binding protein, MeCP2.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP672827.RAI5CSe7WmzzGaH2319SRLSOSsWjgnX-aPrQfHtpgzT9U130_provenance.
• NP672828.RAEMICIqEBA4WqqU0RcuSL16p9rge9bfrvO2mvHDkRKKk130_assertion description "[Most cases of Rett syndrome (RTT) are caused by mutations in the methylated DNA-binding protein, MeCP2.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP672828.RAEMICIqEBA4WqqU0RcuSL16p9rge9bfrvO2mvHDkRKKk130_provenance.
• NP950367.RAq34UA6I5L4-afUco-9gkct6EaigRLvX1TmWOfV610BI130_assertion description "[Most cases of Rett syndrome (RTT) are caused by mutations in the methylated DNA-binding protein, MeCP2.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP950367.RAq34UA6I5L4-afUco-9gkct6EaigRLvX1TmWOfV610BI130_provenance.
• NP672822.RAks7coYGhiEsE4F0AGJkHaw8E2xusDl2cqZAt8tGNg5g130_assertion description "[Most cases of Rett syndrome (RTT) are caused by mutations in the methylated DNA-binding protein, MeCP2.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP672822.RAks7coYGhiEsE4F0AGJkHaw8E2xusDl2cqZAt8tGNg5g130_provenance.
• NP672826.RAjquHezEMuQTwHPNsI8KnTlI1BeS_7hjYaPBfZQZn7gw130_assertion description "[Most cases of Rett syndrome (RTT) are caused by mutations in the methylated DNA-binding protein, MeCP2.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP672826.RAjquHezEMuQTwHPNsI8KnTlI1BeS_7hjYaPBfZQZn7gw130_provenance.
• NP672831.RAi5eU4EDLXMf9_8cKFPvMA4FaJXaS4UYFMkXiI1hK8VM130_assertion description "[Most cases of Rett syndrome (RTT) are caused by mutations in the methylated DNA-binding protein, MeCP2.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP672831.RAi5eU4EDLXMf9_8cKFPvMA4FaJXaS4UYFMkXiI1hK8VM130_provenance.