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Matches in Nanopublications for { ?s ?p "[Ataxia with ocular motor apraxia type 1 (AOA1) is an autosomal recessive cerebellar ataxia (ARCA) associated with oculomotor apraxia, hypoalbuminaemia and hypercholesterolaemia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ?g. }

• NP178209.RAaUp7ho0DsuMoLPawJdh4avEv0Z5otiZVoPvQeE7-wS4130_assertion description "[Ataxia with ocular motor apraxia type 1 (AOA1) is an autosomal recessive cerebellar ataxia (ARCA) associated with oculomotor apraxia, hypoalbuminaemia and hypercholesterolaemia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP178209.RAaUp7ho0DsuMoLPawJdh4avEv0Z5otiZVoPvQeE7-wS4130_provenance.
• NP435333.RAC_goblKyaDfe7DpJqCfnu4iQvLZZcaR9jrHlhcjt10o130_assertion description "[Ataxia with ocular motor apraxia type 1 (AOA1) is an autosomal recessive cerebellar ataxia (ARCA) associated with oculomotor apraxia, hypoalbuminaemia and hypercholesterolaemia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP435333.RAC_goblKyaDfe7DpJqCfnu4iQvLZZcaR9jrHlhcjt10o130_provenance.
• NP235407.RANolmCmmhPQXmPeOSi2R-gKx0ZAZeQKUi0ew7qwIsJIk130_assertion description "[Ataxia with ocular motor apraxia type 1 (AOA1) is an autosomal recessive cerebellar ataxia (ARCA) associated with oculomotor apraxia, hypoalbuminaemia and hypercholesterolaemia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP235407.RANolmCmmhPQXmPeOSi2R-gKx0ZAZeQKUi0ew7qwIsJIk130_provenance.
• NP242179.RAPGi1-7U6w2-lpnqRi0w6XnDQVTcGdHV-AwItpfpBWP4130_assertion description "[Ataxia with ocular motor apraxia type 1 (AOA1) is an autosomal recessive cerebellar ataxia (ARCA) associated with oculomotor apraxia, hypoalbuminaemia and hypercholesterolaemia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP242179.RAPGi1-7U6w2-lpnqRi0w6XnDQVTcGdHV-AwItpfpBWP4130_provenance.
• NP914753.RABq0qxs5GDjn0zBW8ga6TEAax12rruQdj-BnigiyT7qo130_assertion description "[Ataxia with ocular motor apraxia type 1 (AOA1) is an autosomal recessive cerebellar ataxia (ARCA) associated with oculomotor apraxia, hypoalbuminaemia and hypercholesterolaemia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP914753.RABq0qxs5GDjn0zBW8ga6TEAax12rruQdj-BnigiyT7qo130_provenance.
• NP366824.RAGrbRQ-Z-waaQ-T0iFhDsuTdngwK2E9V5mBe9GMbwG5A130_assertion description "[Ataxia with ocular motor apraxia type 1 (AOA1) is an autosomal recessive cerebellar ataxia (ARCA) associated with oculomotor apraxia, hypoalbuminaemia and hypercholesterolaemia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP366824.RAGrbRQ-Z-waaQ-T0iFhDsuTdngwK2E9V5mBe9GMbwG5A130_provenance.
• NP490077.RA0y6qKX-98NuBJ3Lxjk5JuQ0-7U6dgaxy061mD3b4zYU130_assertion description "[Ataxia with ocular motor apraxia type 1 (AOA1) is an autosomal recessive cerebellar ataxia (ARCA) associated with oculomotor apraxia, hypoalbuminaemia and hypercholesterolaemia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP490077.RA0y6qKX-98NuBJ3Lxjk5JuQ0-7U6dgaxy061mD3b4zYU130_provenance.
• NP914834.RAUUdejtYtP9nk1L0vGhenf4gKS7Ap7UbhDn-vOnd_464130_assertion description "[Ataxia with ocular motor apraxia type 1 (AOA1) is an autosomal recessive cerebellar ataxia (ARCA) associated with oculomotor apraxia, hypoalbuminaemia and hypercholesterolaemia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP914834.RAUUdejtYtP9nk1L0vGhenf4gKS7Ap7UbhDn-vOnd_464130_provenance.
• NP914769.RA7SaYL3OWJKajPnJr_hVvVv-ukuNGyJS9g50pipEjrU0130_assertion description "[Ataxia with ocular motor apraxia type 1 (AOA1) is an autosomal recessive cerebellar ataxia (ARCA) associated with oculomotor apraxia, hypoalbuminaemia and hypercholesterolaemia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP914769.RA7SaYL3OWJKajPnJr_hVvVv-ukuNGyJS9g50pipEjrU0130_provenance.
• assertion description "[Ataxia with ocular motor apraxia type 1 (AOA1) is an autosomal recessive cerebellar ataxia (ARCA) associated with oculomotor apraxia, hypoalbuminaemia and hypercholesterolaemia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
• assertion description "[Ataxia with ocular motor apraxia type 1 (AOA1) is an autosomal recessive cerebellar ataxia (ARCA) associated with oculomotor apraxia, hypoalbuminaemia and hypercholesterolaemia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
• assertion description "[Ataxia with ocular motor apraxia type 1 (AOA1) is an autosomal recessive cerebellar ataxia (ARCA) associated with oculomotor apraxia, hypoalbuminaemia and hypercholesterolaemia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
• assertion description "[Ataxia with ocular motor apraxia type 1 (AOA1) is an autosomal recessive cerebellar ataxia (ARCA) associated with oculomotor apraxia, hypoalbuminaemia and hypercholesterolaemia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
• assertion description "[Ataxia with ocular motor apraxia type 1 (AOA1) is an autosomal recessive cerebellar ataxia (ARCA) associated with oculomotor apraxia, hypoalbuminaemia and hypercholesterolaemia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
• assertion description "[Ataxia with ocular motor apraxia type 1 (AOA1) is an autosomal recessive cerebellar ataxia (ARCA) associated with oculomotor apraxia, hypoalbuminaemia and hypercholesterolaemia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
• NP414204.RAIb2SmxH-alZsloj6NDL4VEB1j_zE97_l9JSIVvyaXoU130_assertion description "[Ataxia with ocular motor apraxia type 1 (AOA1) is an autosomal recessive cerebellar ataxia (ARCA) associated with oculomotor apraxia, hypoalbuminaemia and hypercholesterolaemia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP414204.RAIb2SmxH-alZsloj6NDL4VEB1j_zE97_l9JSIVvyaXoU130_provenance.
• NP414207.RAIeVw8Hg3UghYa_QplgYSNSzGHCBKhbe_24Fpqp3Ngc0130_assertion description "[Ataxia with ocular motor apraxia type 1 (AOA1) is an autosomal recessive cerebellar ataxia (ARCA) associated with oculomotor apraxia, hypoalbuminaemia and hypercholesterolaemia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP414207.RAIeVw8Hg3UghYa_QplgYSNSzGHCBKhbe_24Fpqp3Ngc0130_provenance.
• NP914773.RAgQePtwv_40gosSG8uooLT8ZGv81bFAumVPja6OuJMOM130_assertion description "[Ataxia with ocular motor apraxia type 1 (AOA1) is an autosomal recessive cerebellar ataxia (ARCA) associated with oculomotor apraxia, hypoalbuminaemia and hypercholesterolaemia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP914773.RAgQePtwv_40gosSG8uooLT8ZGv81bFAumVPja6OuJMOM130_provenance.
• NP414206.RAtS98cderJSZUBhAFLkcdFPboY_MNdoDjfrf6FNcTDSI130_assertion description "[Ataxia with ocular motor apraxia type 1 (AOA1) is an autosomal recessive cerebellar ataxia (ARCA) associated with oculomotor apraxia, hypoalbuminaemia and hypercholesterolaemia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP414206.RAtS98cderJSZUBhAFLkcdFPboY_MNdoDjfrf6FNcTDSI130_provenance.
• NP414209.RArGB-lmyAlhfKKvSVL3lq48fjqsxJp0yfIESPdqKGPb8130_assertion description "[Ataxia with ocular motor apraxia type 1 (AOA1) is an autosomal recessive cerebellar ataxia (ARCA) associated with oculomotor apraxia, hypoalbuminaemia and hypercholesterolaemia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP414209.RArGB-lmyAlhfKKvSVL3lq48fjqsxJp0yfIESPdqKGPb8130_provenance.