Matches in Nanopublications for { ?s ?p "[Ataxia with oculomotor apraxia type 1 (AOA1) is an autosomal recessive disorder characterized by early-onset cerebellar ataxia, oculomotor apraxia, and peripheral neuropathy.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ?g. }
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- NP305802.RAw5GDJxLMBLeNDnAd8csaGfIvqSgVGtadasVByfveR9g130_assertion description "[Ataxia with oculomotor apraxia type 1 (AOA1) is an autosomal recessive disorder characterized by early-onset cerebellar ataxia, oculomotor apraxia, and peripheral neuropathy.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP305802.RAw5GDJxLMBLeNDnAd8csaGfIvqSgVGtadasVByfveR9g130_provenance.
- NP291972.RAHrkWh1oRVtM1slVjeWb-wVTk6Gflc82ZZpWF7WrG3tY130_assertion description "[Ataxia with oculomotor apraxia type 1 (AOA1) is an autosomal recessive disorder characterized by early-onset cerebellar ataxia, oculomotor apraxia, and peripheral neuropathy.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP291972.RAHrkWh1oRVtM1slVjeWb-wVTk6Gflc82ZZpWF7WrG3tY130_provenance.
- assertion description "[Ataxia with oculomotor apraxia type 1 (AOA1) is an autosomal recessive disorder characterized by early-onset cerebellar ataxia, oculomotor apraxia, and peripheral neuropathy.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
- assertion description "[Ataxia with oculomotor apraxia type 1 (AOA1) is an autosomal recessive disorder characterized by early-onset cerebellar ataxia, oculomotor apraxia, and peripheral neuropathy.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
- assertion description "[Ataxia with oculomotor apraxia type 1 (AOA1) is an autosomal recessive disorder characterized by early-onset cerebellar ataxia, oculomotor apraxia, and peripheral neuropathy.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
- NP472614.RAVluTB4qxADjA-lirNlls30gGlEUCw_d7TXyn24WJO1g130_assertion description "[Ataxia with oculomotor apraxia type 1 (AOA1) is an autosomal recessive disorder characterized by early-onset cerebellar ataxia, oculomotor apraxia, and peripheral neuropathy.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP472614.RAVluTB4qxADjA-lirNlls30gGlEUCw_d7TXyn24WJO1g130_provenance.
- NP914784.RADWoTRxClf8yFdS_93ahLNrdVmaMxGSZM7cwbzcHJ7gY130_assertion description "[Ataxia with oculomotor apraxia type 1 (AOA1) is an autosomal recessive disorder characterized by early-onset cerebellar ataxia, oculomotor apraxia, and peripheral neuropathy.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP914784.RADWoTRxClf8yFdS_93ahLNrdVmaMxGSZM7cwbzcHJ7gY130_provenance.
- NP472615.RA7oNMU0CrIVMW8IdwUEhB4zrtvlfi0aj-4LMbs2fd6gQ130_assertion description "[Ataxia with oculomotor apraxia type 1 (AOA1) is an autosomal recessive disorder characterized by early-onset cerebellar ataxia, oculomotor apraxia, and peripheral neuropathy.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP472615.RA7oNMU0CrIVMW8IdwUEhB4zrtvlfi0aj-4LMbs2fd6gQ130_provenance.