Matches in Nanopublications for { ?s ?p "[Chorea-acanthocytosis (ChAc; OMIM 200150) is a rare autosomal recessive disease with dysfunction of the erythrocyte membrane, presenting with acanthocytes and neurological manifestations characterized by progressive hyperkinesias (chorea, dystonia) and neuropsychological impairment.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ?g. }
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- NP665485.RAR8xUN3RmlLdKKq2ka6RP24NRN-VHUtwxSR4089HLpNo130_assertion description "[Chorea-acanthocytosis (ChAc; OMIM 200150) is a rare autosomal recessive disease with dysfunction of the erythrocyte membrane, presenting with acanthocytes and neurological manifestations characterized by progressive hyperkinesias (chorea, dystonia) and neuropsychological impairment.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP665485.RAR8xUN3RmlLdKKq2ka6RP24NRN-VHUtwxSR4089HLpNo130_provenance.
- NP277692.RAhDPsN6i5g4RpAp4XMjrzSuehDJ5ew4kKa-l_5XlmVdQ130_assertion description "[Chorea-acanthocytosis (ChAc; OMIM 200150) is a rare autosomal recessive disease with dysfunction of the erythrocyte membrane, presenting with acanthocytes and neurological manifestations characterized by progressive hyperkinesias (chorea, dystonia) and neuropsychological impairment.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP277692.RAhDPsN6i5g4RpAp4XMjrzSuehDJ5ew4kKa-l_5XlmVdQ130_provenance.
- NP173363.RA0s2-c7yRWfYQ7ROGq64GJNnUFti6uU3l2LK__sWcufc130_assertion description "[Chorea-acanthocytosis (ChAc; OMIM 200150) is a rare autosomal recessive disease with dysfunction of the erythrocyte membrane, presenting with acanthocytes and neurological manifestations characterized by progressive hyperkinesias (chorea, dystonia) and neuropsychological impairment.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP173363.RA0s2-c7yRWfYQ7ROGq64GJNnUFti6uU3l2LK__sWcufc130_provenance.
- assertion description "[Chorea-acanthocytosis (ChAc; OMIM 200150) is a rare autosomal recessive disease with dysfunction of the erythrocyte membrane, presenting with acanthocytes and neurological manifestations characterized by progressive hyperkinesias (chorea, dystonia) and neuropsychological impairment.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
- assertion description "[Chorea-acanthocytosis (ChAc; OMIM 200150) is a rare autosomal recessive disease with dysfunction of the erythrocyte membrane, presenting with acanthocytes and neurological manifestations characterized by progressive hyperkinesias (chorea, dystonia) and neuropsychological impairment.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
- NP561797.RAdubxLGXIo0DsCDz8SaSMXap4fAu8HowkGMI0ZzJCAp4130_assertion description "[Chorea-acanthocytosis (ChAc; OMIM 200150) is a rare autosomal recessive disease with dysfunction of the erythrocyte membrane, presenting with acanthocytes and neurological manifestations characterized by progressive hyperkinesias (chorea, dystonia) and neuropsychological impairment.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP561797.RAdubxLGXIo0DsCDz8SaSMXap4fAu8HowkGMI0ZzJCAp4130_provenance.
- NP561798.RAbx2dBbCjoVnkNwIjDaAlFAyqY46QodXVEIX8D_onJUw130_assertion description "[Chorea-acanthocytosis (ChAc; OMIM 200150) is a rare autosomal recessive disease with dysfunction of the erythrocyte membrane, presenting with acanthocytes and neurological manifestations characterized by progressive hyperkinesias (chorea, dystonia) and neuropsychological impairment.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP561798.RAbx2dBbCjoVnkNwIjDaAlFAyqY46QodXVEIX8D_onJUw130_provenance.
- NP870168.RAses1ldHfjigaDE8-0XVFJbPwgLq0WU3wbnelhOCoJvU130_assertion description "[Chorea-acanthocytosis (ChAc; OMIM 200150) is a rare autosomal recessive disease with dysfunction of the erythrocyte membrane, presenting with acanthocytes and neurological manifestations characterized by progressive hyperkinesias (chorea, dystonia) and neuropsychological impairment.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP870168.RAses1ldHfjigaDE8-0XVFJbPwgLq0WU3wbnelhOCoJvU130_provenance.
- NP870190.RAJvKxLfH0UOHhWp1bWcBk1zIlSc-GzLFX_vZ_U3whz2k130_assertion description "[Chorea-acanthocytosis (ChAc; OMIM 200150) is a rare autosomal recessive disease with dysfunction of the erythrocyte membrane, presenting with acanthocytes and neurological manifestations characterized by progressive hyperkinesias (chorea, dystonia) and neuropsychological impairment.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP870190.RAJvKxLfH0UOHhWp1bWcBk1zIlSc-GzLFX_vZ_U3whz2k130_provenance.