Nanopublications LDF server

Matches in Nanopublications for { ?s ?p "[Autosomal dominant cerebellar ataxias are a clinical and genetically heterogeneous group of progressive neurodegenerative diseases, at present associated with 22 loci (spinocerebellar ataxia [SCA] 1-SCA8, SCA10-SCA19, SCA21, SCA22, fibroblast growth factor 14 [FGF14]-SCA, and dentatorubral-pallidoluysian atrophy [DRPLA]).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ?g. }

• NP400126.RABSqpRHSJeRQOJ2er4mLVXZ9WW30FDVHmnXVqqDWIHeo130_assertion description "[Autosomal dominant cerebellar ataxias are a clinical and genetically heterogeneous group of progressive neurodegenerative diseases, at present associated with 22 loci (spinocerebellar ataxia [SCA] 1-SCA8, SCA10-SCA19, SCA21, SCA22, fibroblast growth factor 14 [FGF14]-SCA, and dentatorubral-pallidoluysian atrophy [DRPLA]).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP400126.RABSqpRHSJeRQOJ2er4mLVXZ9WW30FDVHmnXVqqDWIHeo130_provenance.
• NP281232.RAeSgjQnfjempUyCclJyL1y-E-DQt3ICsrtShUJZ1IqYI130_assertion description "[Autosomal dominant cerebellar ataxias are a clinical and genetically heterogeneous group of progressive neurodegenerative diseases, at present associated with 22 loci (spinocerebellar ataxia [SCA] 1-SCA8, SCA10-SCA19, SCA21, SCA22, fibroblast growth factor 14 [FGF14]-SCA, and dentatorubral-pallidoluysian atrophy [DRPLA]).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP281232.RAeSgjQnfjempUyCclJyL1y-E-DQt3ICsrtShUJZ1IqYI130_provenance.
• NP281339.RAxRw1_FasoKwVvsN1p5sSgSvTHwi3W4NzgD1FSOGpmcM130_assertion description "[Autosomal dominant cerebellar ataxias are a clinical and genetically heterogeneous group of progressive neurodegenerative diseases, at present associated with 22 loci (spinocerebellar ataxia [SCA] 1-SCA8, SCA10-SCA19, SCA21, SCA22, fibroblast growth factor 14 [FGF14]-SCA, and dentatorubral-pallidoluysian atrophy [DRPLA]).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP281339.RAxRw1_FasoKwVvsN1p5sSgSvTHwi3W4NzgD1FSOGpmcM130_provenance.
• NP681585.RA873g8DlWM2gYbrCABcUOvys-YXkH8O57XF-lXVXflOM130_assertion description "[Autosomal dominant cerebellar ataxias are a clinical and genetically heterogeneous group of progressive neurodegenerative diseases, at present associated with 22 loci (spinocerebellar ataxia [SCA] 1-SCA8, SCA10-SCA19, SCA21, SCA22, fibroblast growth factor 14 [FGF14]-SCA, and dentatorubral-pallidoluysian atrophy [DRPLA]).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP681585.RA873g8DlWM2gYbrCABcUOvys-YXkH8O57XF-lXVXflOM130_provenance.
• assertion description "[Autosomal dominant cerebellar ataxias are a clinical and genetically heterogeneous group of progressive neurodegenerative diseases, at present associated with 22 loci (spinocerebellar ataxia [SCA] 1-SCA8, SCA10-SCA19, SCA21, SCA22, fibroblast growth factor 14 [FGF14]-SCA, and dentatorubral-pallidoluysian atrophy [DRPLA]).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
• assertion description "[Autosomal dominant cerebellar ataxias are a clinical and genetically heterogeneous group of progressive neurodegenerative diseases, at present associated with 22 loci (spinocerebellar ataxia [SCA] 1-SCA8, SCA10-SCA19, SCA21, SCA22, fibroblast growth factor 14 [FGF14]-SCA, and dentatorubral-pallidoluysian atrophy [DRPLA]).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
• NP444472.RA94VunYJPuyTxd6BmZs85x3qpyrBwHzKDi_EEel3Dlj4130_assertion description "[Autosomal dominant cerebellar ataxias are a clinical and genetically heterogeneous group of progressive neurodegenerative diseases, at present associated with 22 loci (spinocerebellar ataxia [SCA] 1-SCA8, SCA10-SCA19, SCA21, SCA22, fibroblast growth factor 14 [FGF14]-SCA, and dentatorubral-pallidoluysian atrophy [DRPLA]).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP444472.RA94VunYJPuyTxd6BmZs85x3qpyrBwHzKDi_EEel3Dlj4130_provenance.
• NP444473.RA87vGf3gM18yc9E7nA3XSXZU-iINOgJVwxaGzOtSn36Y130_assertion description "[Autosomal dominant cerebellar ataxias are a clinical and genetically heterogeneous group of progressive neurodegenerative diseases, at present associated with 22 loci (spinocerebellar ataxia [SCA] 1-SCA8, SCA10-SCA19, SCA21, SCA22, fibroblast growth factor 14 [FGF14]-SCA, and dentatorubral-pallidoluysian atrophy [DRPLA]).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP444473.RA87vGf3gM18yc9E7nA3XSXZU-iINOgJVwxaGzOtSn36Y130_provenance.
• NP444475.RA5aCSTGDbK546y672lE3A4wOVU8MRgkafCpYp27hmW_U130_assertion description "[Autosomal dominant cerebellar ataxias are a clinical and genetically heterogeneous group of progressive neurodegenerative diseases, at present associated with 22 loci (spinocerebellar ataxia [SCA] 1-SCA8, SCA10-SCA19, SCA21, SCA22, fibroblast growth factor 14 [FGF14]-SCA, and dentatorubral-pallidoluysian atrophy [DRPLA]).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP444475.RA5aCSTGDbK546y672lE3A4wOVU8MRgkafCpYp27hmW_U130_provenance.
• NP280911.RAOQla7NuVdLmDIqJ5g1BZ0z1e6vwG-VXHbCyUMc0BMO4130_assertion description "[Autosomal dominant cerebellar ataxias are a clinical and genetically heterogeneous group of progressive neurodegenerative diseases, at present associated with 22 loci (spinocerebellar ataxia [SCA] 1-SCA8, SCA10-SCA19, SCA21, SCA22, fibroblast growth factor 14 [FGF14]-SCA, and dentatorubral-pallidoluysian atrophy [DRPLA]).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP280911.RAOQla7NuVdLmDIqJ5g1BZ0z1e6vwG-VXHbCyUMc0BMO4130_provenance.
• NP444471.RAXVCDV64k6E8nlAZ4BSGhVl4IFuTztHZhe2QHaJTQxHk130_assertion description "[Autosomal dominant cerebellar ataxias are a clinical and genetically heterogeneous group of progressive neurodegenerative diseases, at present associated with 22 loci (spinocerebellar ataxia [SCA] 1-SCA8, SCA10-SCA19, SCA21, SCA22, fibroblast growth factor 14 [FGF14]-SCA, and dentatorubral-pallidoluysian atrophy [DRPLA]).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP444471.RAXVCDV64k6E8nlAZ4BSGhVl4IFuTztHZhe2QHaJTQxHk130_provenance.
• assertion description "[Autosomal dominant cerebellar ataxias are a clinical and genetically heterogeneous group of progressive neurodegenerative diseases, at present associated with 22 loci (spinocerebellar ataxia [SCA] 1-SCA8, SCA10-SCA19, SCA21, SCA22, fibroblast growth factor 14 [FGF14]-SCA, and dentatorubral-pallidoluysian atrophy [DRPLA]).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
• assertion description "[Autosomal dominant cerebellar ataxias are a clinical and genetically heterogeneous group of progressive neurodegenerative diseases, at present associated with 22 loci (spinocerebellar ataxia [SCA] 1-SCA8, SCA10-SCA19, SCA21, SCA22, fibroblast growth factor 14 [FGF14]-SCA, and dentatorubral-pallidoluysian atrophy [DRPLA]).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
• NP444478.RAEEnp_hLn0KNe-3hskOekAuq3rFsEKqcBNFNrnoFIhFk130_assertion description "[Autosomal dominant cerebellar ataxias are a clinical and genetically heterogeneous group of progressive neurodegenerative diseases, at present associated with 22 loci (spinocerebellar ataxia [SCA] 1-SCA8, SCA10-SCA19, SCA21, SCA22, fibroblast growth factor 14 [FGF14]-SCA, and dentatorubral-pallidoluysian atrophy [DRPLA]).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP444478.RAEEnp_hLn0KNe-3hskOekAuq3rFsEKqcBNFNrnoFIhFk130_provenance.
• NP681481.RArCAZ-cb53zPGWa9aKjW0A92VvP1iMHEJ_Z1x4C8AlKU130_assertion description "[Autosomal dominant cerebellar ataxias are a clinical and genetically heterogeneous group of progressive neurodegenerative diseases, at present associated with 22 loci (spinocerebellar ataxia [SCA] 1-SCA8, SCA10-SCA19, SCA21, SCA22, fibroblast growth factor 14 [FGF14]-SCA, and dentatorubral-pallidoluysian atrophy [DRPLA]).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP681481.RArCAZ-cb53zPGWa9aKjW0A92VvP1iMHEJ_Z1x4C8AlKU130_provenance.
• NP444476.RAmgnPxZhfWQNW8hEo3qp7eCqar_rPgO7QL8h3eYjdnWU130_assertion description "[Autosomal dominant cerebellar ataxias are a clinical and genetically heterogeneous group of progressive neurodegenerative diseases, at present associated with 22 loci (spinocerebellar ataxia [SCA] 1-SCA8, SCA10-SCA19, SCA21, SCA22, fibroblast growth factor 14 [FGF14]-SCA, and dentatorubral-pallidoluysian atrophy [DRPLA]).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP444476.RAmgnPxZhfWQNW8hEo3qp7eCqar_rPgO7QL8h3eYjdnWU130_provenance.
• NP444477.RAjoCriUdFBvSIGYhj85GZSuEe13uxkwygwHGpqfCyKrg130_assertion description "[Autosomal dominant cerebellar ataxias are a clinical and genetically heterogeneous group of progressive neurodegenerative diseases, at present associated with 22 loci (spinocerebellar ataxia [SCA] 1-SCA8, SCA10-SCA19, SCA21, SCA22, fibroblast growth factor 14 [FGF14]-SCA, and dentatorubral-pallidoluysian atrophy [DRPLA]).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP444477.RAjoCriUdFBvSIGYhj85GZSuEe13uxkwygwHGpqfCyKrg130_provenance.