Nanopublications LDF server

Matches in Nanopublications for { ?s ?p "[Myoclonus-dystonia is a movement disorder associated with mutations in the epsilon-sarcoglycan gene (SGCE) in most families and in the DRD2 and DYT1 genes in two single families.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ?g. }

• NP133076.RABV6G8Gzbpc1o1ShIz33P82zocJjWHXM1_AzYOqVqBhg130_assertion description "[Myoclonus-dystonia is a movement disorder associated with mutations in the epsilon-sarcoglycan gene (SGCE) in most families and in the DRD2 and DYT1 genes in two single families.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP133076.RABV6G8Gzbpc1o1ShIz33P82zocJjWHXM1_AzYOqVqBhg130_provenance.
• NP884994.RABFxtgp6hIY9eEe2c6hlxiBCULJCIPBmkAuws1Xev5Aw130_assertion description "[Myoclonus-dystonia is a movement disorder associated with mutations in the epsilon-sarcoglycan gene (SGCE) in most families and in the DRD2 and DYT1 genes in two single families.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP884994.RABFxtgp6hIY9eEe2c6hlxiBCULJCIPBmkAuws1Xev5Aw130_provenance.
• NP184624.RA69LznUyW80ITQ4TUwYW8g4U8UrgMD5AnWCzZRr4oyfM130_assertion description "[Myoclonus-dystonia is a movement disorder associated with mutations in the epsilon-sarcoglycan gene (SGCE) in most families and in the DRD2 and DYT1 genes in two single families.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP184624.RA69LznUyW80ITQ4TUwYW8g4U8UrgMD5AnWCzZRr4oyfM130_provenance.
• NP205886.RA_cuR9CWy303BZcnjOSy33l66C4t47kee_X8_4wEXMVk130_assertion description "[Myoclonus-dystonia is a movement disorder associated with mutations in the epsilon-sarcoglycan gene (SGCE) in most families and in the DRD2 and DYT1 genes in two single families.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP205886.RA_cuR9CWy303BZcnjOSy33l66C4t47kee_X8_4wEXMVk130_provenance.
• NP792903.RAA1uFoXg6Ewjp7lTy170NLx99ujpF9O7yZxBGLAJ8cVY130_assertion description "[Myoclonus-dystonia is a movement disorder associated with mutations in the epsilon-sarcoglycan gene (SGCE) in most families and in the DRD2 and DYT1 genes in two single families.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP792903.RAA1uFoXg6Ewjp7lTy170NLx99ujpF9O7yZxBGLAJ8cVY130_provenance.
• NP414827.RAYL1Nc4t1cZvr6Q06uZB8Sd4fkzqKSfQtCN4nwq3pmzM130_assertion description "[Myoclonus-dystonia is a movement disorder associated with mutations in the epsilon-sarcoglycan gene (SGCE) in most families and in the DRD2 and DYT1 genes in two single families.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP414827.RAYL1Nc4t1cZvr6Q06uZB8Sd4fkzqKSfQtCN4nwq3pmzM130_provenance.
• NP615762.RAk9ZOHzmmpEXdZGwBiVZJsEORzo3mo1sQfrlPhAoMeqk130_assertion description "[Myoclonus-dystonia is a movement disorder associated with mutations in the epsilon-sarcoglycan gene (SGCE) in most families and in the DRD2 and DYT1 genes in two single families.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP615762.RAk9ZOHzmmpEXdZGwBiVZJsEORzo3mo1sQfrlPhAoMeqk130_provenance.
• assertion description "[Myoclonus-dystonia is a movement disorder associated with mutations in the epsilon-sarcoglycan gene (SGCE) in most families and in the DRD2 and DYT1 genes in two single families.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
• assertion description "[Myoclonus-dystonia is a movement disorder associated with mutations in the epsilon-sarcoglycan gene (SGCE) in most families and in the DRD2 and DYT1 genes in two single families.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
• assertion description "[Myoclonus-dystonia is a movement disorder associated with mutations in the epsilon-sarcoglycan gene (SGCE) in most families and in the DRD2 and DYT1 genes in two single families.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
• assertion description "[Myoclonus-dystonia is a movement disorder associated with mutations in the epsilon-sarcoglycan gene (SGCE) in most families and in the DRD2 and DYT1 genes in two single families.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
• NP405388.RA-KbvznTBHaFXaqyhqcajRwkhhf2lIKtNyZaCe5GDMLY130_assertion description "[Myoclonus-dystonia is a movement disorder associated with mutations in the epsilon-sarcoglycan gene (SGCE) in most families and in the DRD2 and DYT1 genes in two single families.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP405388.RA-KbvznTBHaFXaqyhqcajRwkhhf2lIKtNyZaCe5GDMLY130_provenance.
• NP196236.RAaup9iLZsYivb-fTOkWK2YtLxMou6OYEHtLJSuBH9yig130_assertion description "[Myoclonus-dystonia is a movement disorder associated with mutations in the epsilon-sarcoglycan gene (SGCE) in most families and in the DRD2 and DYT1 genes in two single families.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP196236.RAaup9iLZsYivb-fTOkWK2YtLxMou6OYEHtLJSuBH9yig130_provenance.
• NP362908.RATvpib7cTXQPDJfJv27rcgB61Fys75amBaaCZbIU3kLQ130_assertion description "[Myoclonus-dystonia is a movement disorder associated with mutations in the epsilon-sarcoglycan gene (SGCE) in most families and in the DRD2 and DYT1 genes in two single families.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP362908.RATvpib7cTXQPDJfJv27rcgB61Fys75amBaaCZbIU3kLQ130_provenance.
• NP810920.RAU2pnlQvhyDagUJ5BKbp3ZXIB114zFAB1WJ8esE-HQLs130_assertion description "[Myoclonus-dystonia is a movement disorder associated with mutations in the epsilon-sarcoglycan gene (SGCE) in most families and in the DRD2 and DYT1 genes in two single families.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP810920.RAU2pnlQvhyDagUJ5BKbp3ZXIB114zFAB1WJ8esE-HQLs130_provenance.
• NP248.RA9jK2QD-D-VHQUIcu7UyevJ419jFiSeHOiGsiMBA3vBU130_assertion description "[Myoclonus-dystonia is a movement disorder associated with mutations in the epsilon-sarcoglycan gene (SGCE) in most families and in the DRD2 and DYT1 genes in two single families.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP248.RA9jK2QD-D-VHQUIcu7UyevJ419jFiSeHOiGsiMBA3vBU130_provenance.
• NP482464.RANojDp066YmCWKqIMZGQ59NI1boS85NMI2kJEFte2iNo130_assertion description "[Myoclonus-dystonia is a movement disorder associated with mutations in the epsilon-sarcoglycan gene (SGCE) in most families and in the DRD2 and DYT1 genes in two single families.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP482464.RANojDp066YmCWKqIMZGQ59NI1boS85NMI2kJEFte2iNo130_provenance.
• NP2338.RASnnHXeBPO_BIdlp1nvv1WSPou7AYf2ioIpMdyOveUqc130_assertion description "[Myoclonus-dystonia is a movement disorder associated with mutations in the epsilon-sarcoglycan gene (SGCE) in most families and in the DRD2 and DYT1 genes in two single families.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP2338.RASnnHXeBPO_BIdlp1nvv1WSPou7AYf2ioIpMdyOveUqc130_provenance.
• assertion description "[Myoclonus-dystonia is a movement disorder associated with mutations in the epsilon-sarcoglycan gene (SGCE) in most families and in the DRD2 and DYT1 genes in two single families.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
• assertion description "[Myoclonus-dystonia is a movement disorder associated with mutations in the epsilon-sarcoglycan gene (SGCE) in most families and in the DRD2 and DYT1 genes in two single families.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
• assertion description "[Myoclonus-dystonia is a movement disorder associated with mutations in the epsilon-sarcoglycan gene (SGCE) in most families and in the DRD2 and DYT1 genes in two single families.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
• assertion description "[Myoclonus-dystonia is a movement disorder associated with mutations in the epsilon-sarcoglycan gene (SGCE) in most families and in the DRD2 and DYT1 genes in two single families.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
• NP372539.RATYb2zbEo2nDixOe_DNNUEEc6sRnkG1Cch2arj_f902k130_assertion description "[Myoclonus-dystonia is a movement disorder associated with mutations in the epsilon-sarcoglycan gene (SGCE) in most families and in the DRD2 and DYT1 genes in two single families.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP372539.RATYb2zbEo2nDixOe_DNNUEEc6sRnkG1Cch2arj_f902k130_provenance.
• NP372536.RAkpldmLPtZ2I15n3GiF6t96FrSxZEc1ZJAkT3ksQdJ_8130_assertion description "[Myoclonus-dystonia is a movement disorder associated with mutations in the epsilon-sarcoglycan gene (SGCE) in most families and in the DRD2 and DYT1 genes in two single families.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP372536.RAkpldmLPtZ2I15n3GiF6t96FrSxZEc1ZJAkT3ksQdJ_8130_provenance.
• NP372538.RAoV5P4WtvNfobGW7AMY5CmlExWANMzfvqrCmcKkuoiVU130_assertion description "[Myoclonus-dystonia is a movement disorder associated with mutations in the epsilon-sarcoglycan gene (SGCE) in most families and in the DRD2 and DYT1 genes in two single families.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP372538.RAoV5P4WtvNfobGW7AMY5CmlExWANMzfvqrCmcKkuoiVU130_provenance.
• NP372540.RAqCssnEqs6azb2GuQpvlCWWeHw6xPHC7-J5JBbeH_As0130_assertion description "[Myoclonus-dystonia is a movement disorder associated with mutations in the epsilon-sarcoglycan gene (SGCE) in most families and in the DRD2 and DYT1 genes in two single families.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP372540.RAqCssnEqs6azb2GuQpvlCWWeHw6xPHC7-J5JBbeH_As0130_provenance.
• NP359582.RAzmi5W3wWlBG8KJqRCC3MzPuVyhoeb1ufAp_XqwBXZ2s130_assertion description "[Myoclonus-dystonia is a movement disorder associated with mutations in the epsilon-sarcoglycan gene (SGCE) in most families and in the DRD2 and DYT1 genes in two single families.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP359582.RAzmi5W3wWlBG8KJqRCC3MzPuVyhoeb1ufAp_XqwBXZ2s130_provenance.
• NP359986.RAxzxwwVyv7TsRsDTdukdrFlDxgrtCxkCVJXY786xktn8130_assertion description "[Myoclonus-dystonia is a movement disorder associated with mutations in the epsilon-sarcoglycan gene (SGCE) in most families and in the DRD2 and DYT1 genes in two single families.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP359986.RAxzxwwVyv7TsRsDTdukdrFlDxgrtCxkCVJXY786xktn8130_provenance.
• NP196797.RAF9WPWcPWl4yeaUKkvnh_lrv3qAf8ovbgAsN404UOTVc130_assertion description "[Myoclonus-dystonia is a movement disorder associated with mutations in the epsilon-sarcoglycan gene (SGCE) in most families and in the DRD2 and DYT1 genes in two single families.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP196797.RAF9WPWcPWl4yeaUKkvnh_lrv3qAf8ovbgAsN404UOTVc130_provenance.
• NP372537.RA7Qqtr26OYBBlUKvg2C93drZfy3MnFuq24Xq2CSSTFZY130_assertion description "[Myoclonus-dystonia is a movement disorder associated with mutations in the epsilon-sarcoglycan gene (SGCE) in most families and in the DRD2 and DYT1 genes in two single families.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP372537.RA7Qqtr26OYBBlUKvg2C93drZfy3MnFuq24Xq2CSSTFZY130_provenance.
• NP372541.RA_nCNsK-OkoG6q6A160DgOrCGBgD_3DyqKDSzgHF9amQ130_assertion description "[Myoclonus-dystonia is a movement disorder associated with mutations in the epsilon-sarcoglycan gene (SGCE) in most families and in the DRD2 and DYT1 genes in two single families.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP372541.RA_nCNsK-OkoG6q6A160DgOrCGBgD_3DyqKDSzgHF9amQ130_provenance.