Matches in Nanopublications for { ?s ?p "[Mutations of the aprataxin (APTX) gene cause early-onset ataxia with ocular motor apraxia and hypoalbuminemia (EAOH), also called ataxia with oculomotor apraxia type 1.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ?g. }
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- NP347274.RAoLKuPB8tPBhnmedKNAcQ9QLTAtUXM845AQhWcm3zvSk130_assertion description "[Mutations of the aprataxin (APTX) gene cause early-onset ataxia with ocular motor apraxia and hypoalbuminemia (EAOH), also called ataxia with oculomotor apraxia type 1.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP347274.RAoLKuPB8tPBhnmedKNAcQ9QLTAtUXM845AQhWcm3zvSk130_provenance.
- NP207934.RAQdNCsOsVFQSFQai6MMGqaceJXZdg4J8bhU2p6VISbJA130_assertion description "[Mutations of the aprataxin (APTX) gene cause early-onset ataxia with ocular motor apraxia and hypoalbuminemia (EAOH), also called ataxia with oculomotor apraxia type 1.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP207934.RAQdNCsOsVFQSFQai6MMGqaceJXZdg4J8bhU2p6VISbJA130_provenance.
- NP288046.RA6g76Sp7lTZsZBzaQ0pMZ2C_hcJSITivnuOi_prZY8yo130_assertion description "[Mutations of the aprataxin (APTX) gene cause early-onset ataxia with ocular motor apraxia and hypoalbuminemia (EAOH), also called ataxia with oculomotor apraxia type 1.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP288046.RA6g76Sp7lTZsZBzaQ0pMZ2C_hcJSITivnuOi_prZY8yo130_provenance.
- NP914827.RAeHb7nJHxgB75JyRX2j_p9SK8sQSWjTghF0VPVXsLFiI130_assertion description "[Mutations of the aprataxin (APTX) gene cause early-onset ataxia with ocular motor apraxia and hypoalbuminemia (EAOH), also called ataxia with oculomotor apraxia type 1.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP914827.RAeHb7nJHxgB75JyRX2j_p9SK8sQSWjTghF0VPVXsLFiI130_provenance.
- assertion description "[Mutations of the aprataxin (APTX) gene cause early-onset ataxia with ocular motor apraxia and hypoalbuminemia (EAOH), also called ataxia with oculomotor apraxia type 1.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
- assertion description "[Mutations of the aprataxin (APTX) gene cause early-onset ataxia with ocular motor apraxia and hypoalbuminemia (EAOH), also called ataxia with oculomotor apraxia type 1.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
- NP575020.RAXYgraOF0HgcaybI13l_j7S2nC5S_nvblRMXPfpDDxDk130_assertion description "[Mutations of the aprataxin (APTX) gene cause early-onset ataxia with ocular motor apraxia and hypoalbuminemia (EAOH), also called ataxia with oculomotor apraxia type 1.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP575020.RAXYgraOF0HgcaybI13l_j7S2nC5S_nvblRMXPfpDDxDk130_provenance.
- NP914811.RApnHe3c2drqwcXPOp4BvlJ1mvtSUXvmkdtb1YXqp0bCQ130_assertion description "[Mutations of the aprataxin (APTX) gene cause early-onset ataxia with ocular motor apraxia and hypoalbuminemia (EAOH), also called ataxia with oculomotor apraxia type 1.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP914811.RApnHe3c2drqwcXPOp4BvlJ1mvtSUXvmkdtb1YXqp0bCQ130_provenance.
- NP575017.RALxXQcKpUXS_YsItkZ30M8x7Z-VrBAaQi4pf41qKCyw4130_assertion description "[Mutations of the aprataxin (APTX) gene cause early-onset ataxia with ocular motor apraxia and hypoalbuminemia (EAOH), also called ataxia with oculomotor apraxia type 1.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP575017.RALxXQcKpUXS_YsItkZ30M8x7Z-VrBAaQi4pf41qKCyw4130_provenance.