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Matches in Nanopublications for { ?s ?p "[Dominantly transmitted cases had (CAG)(n) expansions at the Machado-Joseph disease gene (MJD1) (63%), at SCA2 (3%), the gene for dentatorubropallidoluysian atrophy (DRPLA) (2%), SCA6 (1%), or SCA7 (1%) loci, or (CTG)(n) expansions at the SCA8 (2%) gene, whereas (GAA)(n) expansions in the Freidreich ataxia gene (FRDA) were found in 64% of families with recessive ataxia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ?g. }

• NP923897.RAfTRsIZNANT-uGz-3pWkBRBrjk24o-JZKP7RcHvG_eo8130_assertion description "[Dominantly transmitted cases had (CAG)(n) expansions at the Machado-Joseph disease gene (MJD1) (63%), at SCA2 (3%), the gene for dentatorubropallidoluysian atrophy (DRPLA) (2%), SCA6 (1%), or SCA7 (1%) loci, or (CTG)(n) expansions at the SCA8 (2%) gene, whereas (GAA)(n) expansions in the Freidreich ataxia gene (FRDA) were found in 64% of families with recessive ataxia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP923897.RAfTRsIZNANT-uGz-3pWkBRBrjk24o-JZKP7RcHvG_eo8130_provenance.
• NP276991.RASpjW0gfj6Fi-nksphtMaYwj2GYK_XnTSuj909vNq_8Y130_assertion description "[Dominantly transmitted cases had (CAG)(n) expansions at the Machado-Joseph disease gene (MJD1) (63%), at SCA2 (3%), the gene for dentatorubropallidoluysian atrophy (DRPLA) (2%), SCA6 (1%), or SCA7 (1%) loci, or (CTG)(n) expansions at the SCA8 (2%) gene, whereas (GAA)(n) expansions in the Freidreich ataxia gene (FRDA) were found in 64% of families with recessive ataxia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP276991.RASpjW0gfj6Fi-nksphtMaYwj2GYK_XnTSuj909vNq_8Y130_provenance.
• NP277152.RAcy20gQdKTkdcLTTBSH3nvsWFCw_gMZRFQ5-3phiOh5I130_assertion description "[Dominantly transmitted cases had (CAG)(n) expansions at the Machado-Joseph disease gene (MJD1) (63%), at SCA2 (3%), the gene for dentatorubropallidoluysian atrophy (DRPLA) (2%), SCA6 (1%), or SCA7 (1%) loci, or (CTG)(n) expansions at the SCA8 (2%) gene, whereas (GAA)(n) expansions in the Freidreich ataxia gene (FRDA) were found in 64% of families with recessive ataxia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP277152.RAcy20gQdKTkdcLTTBSH3nvsWFCw_gMZRFQ5-3phiOh5I130_provenance.
• NP682025.RAfCfKH0Esw9H69dA10LeQ-oQUwcGwLPyh2Z8W_cBAtWE130_assertion description "[Dominantly transmitted cases had (CAG)(n) expansions at the Machado-Joseph disease gene (MJD1) (63%), at SCA2 (3%), the gene for dentatorubropallidoluysian atrophy (DRPLA) (2%), SCA6 (1%), or SCA7 (1%) loci, or (CTG)(n) expansions at the SCA8 (2%) gene, whereas (GAA)(n) expansions in the Freidreich ataxia gene (FRDA) were found in 64% of families with recessive ataxia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP682025.RAfCfKH0Esw9H69dA10LeQ-oQUwcGwLPyh2Z8W_cBAtWE130_provenance.
• NP351109.RAcoKkpTi2WGn4RRWkSNr1sXCpFIGGQX15_aWgEApnbGc130_assertion description "[Dominantly transmitted cases had (CAG)(n) expansions at the Machado-Joseph disease gene (MJD1) (63%), at SCA2 (3%), the gene for dentatorubropallidoluysian atrophy (DRPLA) (2%), SCA6 (1%), or SCA7 (1%) loci, or (CTG)(n) expansions at the SCA8 (2%) gene, whereas (GAA)(n) expansions in the Freidreich ataxia gene (FRDA) were found in 64% of families with recessive ataxia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP351109.RAcoKkpTi2WGn4RRWkSNr1sXCpFIGGQX15_aWgEApnbGc130_provenance.
• NP351111.RAbnhX0RHlVIEiFPFK_i5eMHVOY3-bxmqjyM4BsJtNsDA130_assertion description "[Dominantly transmitted cases had (CAG)(n) expansions at the Machado-Joseph disease gene (MJD1) (63%), at SCA2 (3%), the gene for dentatorubropallidoluysian atrophy (DRPLA) (2%), SCA6 (1%), or SCA7 (1%) loci, or (CTG)(n) expansions at the SCA8 (2%) gene, whereas (GAA)(n) expansions in the Freidreich ataxia gene (FRDA) were found in 64% of families with recessive ataxia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP351111.RAbnhX0RHlVIEiFPFK_i5eMHVOY3-bxmqjyM4BsJtNsDA130_provenance.
• NP351113.RAcENZcn-hOEoSMtwtm8RySszoHE0dcZXMJJA9R8ZbZKU130_assertion description "[Dominantly transmitted cases had (CAG)(n) expansions at the Machado-Joseph disease gene (MJD1) (63%), at SCA2 (3%), the gene for dentatorubropallidoluysian atrophy (DRPLA) (2%), SCA6 (1%), or SCA7 (1%) loci, or (CTG)(n) expansions at the SCA8 (2%) gene, whereas (GAA)(n) expansions in the Freidreich ataxia gene (FRDA) were found in 64% of families with recessive ataxia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP351113.RAcENZcn-hOEoSMtwtm8RySszoHE0dcZXMJJA9R8ZbZKU130_provenance.
• NP351116.RAY3fKtisuB5do-aUlWwEF_T9JH7m0bmRtikUuSC7wS64130_assertion description "[Dominantly transmitted cases had (CAG)(n) expansions at the Machado-Joseph disease gene (MJD1) (63%), at SCA2 (3%), the gene for dentatorubropallidoluysian atrophy (DRPLA) (2%), SCA6 (1%), or SCA7 (1%) loci, or (CTG)(n) expansions at the SCA8 (2%) gene, whereas (GAA)(n) expansions in the Freidreich ataxia gene (FRDA) were found in 64% of families with recessive ataxia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP351116.RAY3fKtisuB5do-aUlWwEF_T9JH7m0bmRtikUuSC7wS64130_provenance.
• NP681710.RAq8QiOZEbUYOlebcpncIdx-gvLXuYdJG4twxrZf6moNQ130_assertion description "[Dominantly transmitted cases had (CAG)(n) expansions at the Machado-Joseph disease gene (MJD1) (63%), at SCA2 (3%), the gene for dentatorubropallidoluysian atrophy (DRPLA) (2%), SCA6 (1%), or SCA7 (1%) loci, or (CTG)(n) expansions at the SCA8 (2%) gene, whereas (GAA)(n) expansions in the Freidreich ataxia gene (FRDA) were found in 64% of families with recessive ataxia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP681710.RAq8QiOZEbUYOlebcpncIdx-gvLXuYdJG4twxrZf6moNQ130_provenance.
• NP351107.RAmClFX4KhW9y5efqMR5uVoKc0q0TxRzeY6_tx2KGocG8130_assertion description "[Dominantly transmitted cases had (CAG)(n) expansions at the Machado-Joseph disease gene (MJD1) (63%), at SCA2 (3%), the gene for dentatorubropallidoluysian atrophy (DRPLA) (2%), SCA6 (1%), or SCA7 (1%) loci, or (CTG)(n) expansions at the SCA8 (2%) gene, whereas (GAA)(n) expansions in the Freidreich ataxia gene (FRDA) were found in 64% of families with recessive ataxia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP351107.RAmClFX4KhW9y5efqMR5uVoKc0q0TxRzeY6_tx2KGocG8130_provenance.
• NP351108.RAjUWaFwEsYrubH04788Fl6YJQIhqdZ3yz5uBuM3d8tfo130_assertion description "[Dominantly transmitted cases had (CAG)(n) expansions at the Machado-Joseph disease gene (MJD1) (63%), at SCA2 (3%), the gene for dentatorubropallidoluysian atrophy (DRPLA) (2%), SCA6 (1%), or SCA7 (1%) loci, or (CTG)(n) expansions at the SCA8 (2%) gene, whereas (GAA)(n) expansions in the Freidreich ataxia gene (FRDA) were found in 64% of families with recessive ataxia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP351108.RAjUWaFwEsYrubH04788Fl6YJQIhqdZ3yz5uBuM3d8tfo130_provenance.
• NP351121.RAtI_GWEzt5DjXcD0I1pCmCWYYiql_yUNDJhM3x7ykeG0130_assertion description "[Dominantly transmitted cases had (CAG)(n) expansions at the Machado-Joseph disease gene (MJD1) (63%), at SCA2 (3%), the gene for dentatorubropallidoluysian atrophy (DRPLA) (2%), SCA6 (1%), or SCA7 (1%) loci, or (CTG)(n) expansions at the SCA8 (2%) gene, whereas (GAA)(n) expansions in the Freidreich ataxia gene (FRDA) were found in 64% of families with recessive ataxia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP351121.RAtI_GWEzt5DjXcD0I1pCmCWYYiql_yUNDJhM3x7ykeG0130_provenance.
• NP541641.RAI0jgRAAk1nFEWSD_R6fuzZsO6z9WyealBERi8tKBk9k130_assertion description "[Dominantly transmitted cases had (CAG)(n) expansions at the Machado-Joseph disease gene (MJD1) (63%), at SCA2 (3%), the gene for dentatorubropallidoluysian atrophy (DRPLA) (2%), SCA6 (1%), or SCA7 (1%) loci, or (CTG)(n) expansions at the SCA8 (2%) gene, whereas (GAA)(n) expansions in the Freidreich ataxia gene (FRDA) were found in 64% of families with recessive ataxia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP541641.RAI0jgRAAk1nFEWSD_R6fuzZsO6z9WyealBERi8tKBk9k130_provenance.
• NP541719.RA4YdKBXXdtdlTuaFXjLJ6JP_GNIU_eQK6wi-vVMeKinI130_assertion description "[Dominantly transmitted cases had (CAG)(n) expansions at the Machado-Joseph disease gene (MJD1) (63%), at SCA2 (3%), the gene for dentatorubropallidoluysian atrophy (DRPLA) (2%), SCA6 (1%), or SCA7 (1%) loci, or (CTG)(n) expansions at the SCA8 (2%) gene, whereas (GAA)(n) expansions in the Freidreich ataxia gene (FRDA) were found in 64% of families with recessive ataxia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP541719.RA4YdKBXXdtdlTuaFXjLJ6JP_GNIU_eQK6wi-vVMeKinI130_provenance.
• NP351106.RAKzun82mVNuHVs4Ap6J0AiE47486pkNAukpfukcyCD7I130_assertion description "[Dominantly transmitted cases had (CAG)(n) expansions at the Machado-Joseph disease gene (MJD1) (63%), at SCA2 (3%), the gene for dentatorubropallidoluysian atrophy (DRPLA) (2%), SCA6 (1%), or SCA7 (1%) loci, or (CTG)(n) expansions at the SCA8 (2%) gene, whereas (GAA)(n) expansions in the Freidreich ataxia gene (FRDA) were found in 64% of families with recessive ataxia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP351106.RAKzun82mVNuHVs4Ap6J0AiE47486pkNAukpfukcyCD7I130_provenance.
• NP351115.RAJ1eq9cw62SGaVujUMwm9fKS01misAuy48lapv-nZNe0130_assertion description "[Dominantly transmitted cases had (CAG)(n) expansions at the Machado-Joseph disease gene (MJD1) (63%), at SCA2 (3%), the gene for dentatorubropallidoluysian atrophy (DRPLA) (2%), SCA6 (1%), or SCA7 (1%) loci, or (CTG)(n) expansions at the SCA8 (2%) gene, whereas (GAA)(n) expansions in the Freidreich ataxia gene (FRDA) were found in 64% of families with recessive ataxia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP351115.RAJ1eq9cw62SGaVujUMwm9fKS01misAuy48lapv-nZNe0130_provenance.
• NP351118.RANzr552nAuaCJ3_Kv9NlsFvjMG6iASWWcELUMQsemRRE130_assertion description "[Dominantly transmitted cases had (CAG)(n) expansions at the Machado-Joseph disease gene (MJD1) (63%), at SCA2 (3%), the gene for dentatorubropallidoluysian atrophy (DRPLA) (2%), SCA6 (1%), or SCA7 (1%) loci, or (CTG)(n) expansions at the SCA8 (2%) gene, whereas (GAA)(n) expansions in the Freidreich ataxia gene (FRDA) were found in 64% of families with recessive ataxia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP351118.RANzr552nAuaCJ3_Kv9NlsFvjMG6iASWWcELUMQsemRRE130_provenance.
• NP681816.RAF3KN1c9zujIUgeEBBHDm7GmHFJ8NzYpZSRCIUN7tAgA130_assertion description "[Dominantly transmitted cases had (CAG)(n) expansions at the Machado-Joseph disease gene (MJD1) (63%), at SCA2 (3%), the gene for dentatorubropallidoluysian atrophy (DRPLA) (2%), SCA6 (1%), or SCA7 (1%) loci, or (CTG)(n) expansions at the SCA8 (2%) gene, whereas (GAA)(n) expansions in the Freidreich ataxia gene (FRDA) were found in 64% of families with recessive ataxia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP681816.RAF3KN1c9zujIUgeEBBHDm7GmHFJ8NzYpZSRCIUN7tAgA130_provenance.
• NP681880.RA5TdN6BwDTuE-hiM95KUbkdIz-ksh-CfuCCLzRGHNi6U130_assertion description "[Dominantly transmitted cases had (CAG)(n) expansions at the Machado-Joseph disease gene (MJD1) (63%), at SCA2 (3%), the gene for dentatorubropallidoluysian atrophy (DRPLA) (2%), SCA6 (1%), or SCA7 (1%) loci, or (CTG)(n) expansions at the SCA8 (2%) gene, whereas (GAA)(n) expansions in the Freidreich ataxia gene (FRDA) were found in 64% of families with recessive ataxia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP681880.RA5TdN6BwDTuE-hiM95KUbkdIz-ksh-CfuCCLzRGHNi6U130_provenance.
• NP681940.RAzi9qX2-IPRY8o4FGtG74AJya4WNxo-1LVoLGquVQiNA130_assertion description "[Dominantly transmitted cases had (CAG)(n) expansions at the Machado-Joseph disease gene (MJD1) (63%), at SCA2 (3%), the gene for dentatorubropallidoluysian atrophy (DRPLA) (2%), SCA6 (1%), or SCA7 (1%) loci, or (CTG)(n) expansions at the SCA8 (2%) gene, whereas (GAA)(n) expansions in the Freidreich ataxia gene (FRDA) were found in 64% of families with recessive ataxia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP681940.RAzi9qX2-IPRY8o4FGtG74AJya4WNxo-1LVoLGquVQiNA130_provenance.
• NP351105.RA7jp3nPqAX_1qZoeHwS_AY0-UcZgcmx7FGeWOirpmyWc130_assertion description "[Dominantly transmitted cases had (CAG)(n) expansions at the Machado-Joseph disease gene (MJD1) (63%), at SCA2 (3%), the gene for dentatorubropallidoluysian atrophy (DRPLA) (2%), SCA6 (1%), or SCA7 (1%) loci, or (CTG)(n) expansions at the SCA8 (2%) gene, whereas (GAA)(n) expansions in the Freidreich ataxia gene (FRDA) were found in 64% of families with recessive ataxia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP351105.RA7jp3nPqAX_1qZoeHwS_AY0-UcZgcmx7FGeWOirpmyWc130_provenance.
• NP351110.RA8n8xVSn4_3NM1GqckAogVpV-H3CZdXa72fyhsRUMh7I130_assertion description "[Dominantly transmitted cases had (CAG)(n) expansions at the Machado-Joseph disease gene (MJD1) (63%), at SCA2 (3%), the gene for dentatorubropallidoluysian atrophy (DRPLA) (2%), SCA6 (1%), or SCA7 (1%) loci, or (CTG)(n) expansions at the SCA8 (2%) gene, whereas (GAA)(n) expansions in the Freidreich ataxia gene (FRDA) were found in 64% of families with recessive ataxia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP351110.RA8n8xVSn4_3NM1GqckAogVpV-H3CZdXa72fyhsRUMh7I130_provenance.
• NP351114.RA20sbzVX6Ivizud4pvS1lqOguAFtHh0YUIvTIKm2mvBE130_assertion description "[Dominantly transmitted cases had (CAG)(n) expansions at the Machado-Joseph disease gene (MJD1) (63%), at SCA2 (3%), the gene for dentatorubropallidoluysian atrophy (DRPLA) (2%), SCA6 (1%), or SCA7 (1%) loci, or (CTG)(n) expansions at the SCA8 (2%) gene, whereas (GAA)(n) expansions in the Freidreich ataxia gene (FRDA) were found in 64% of families with recessive ataxia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP351114.RA20sbzVX6Ivizud4pvS1lqOguAFtHh0YUIvTIKm2mvBE130_provenance.