Matches in Nanopublications for { ?s ?p "[Spinocerebellar ataxia type 1 (SCA1) is an adult-onset, dominantly inherited neurodegenerative disease caused by expansion of a glutamine repeat tract in ataxin-1 (ATXN1).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ?g. }
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- NP484500.RASWoA7jYU8ciFtk_ZXyFdQhBkkI84lh-APhLY9WWVcZI130_assertion description "[Spinocerebellar ataxia type 1 (SCA1) is an adult-onset, dominantly inherited neurodegenerative disease caused by expansion of a glutamine repeat tract in ataxin-1 (ATXN1).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP484500.RASWoA7jYU8ciFtk_ZXyFdQhBkkI84lh-APhLY9WWVcZI130_provenance.
- assertion description "[Spinocerebellar ataxia type 1 (SCA1) is an adult-onset, dominantly inherited neurodegenerative disease caused by expansion of a glutamine repeat tract in ataxin-1 (ATXN1).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
- NP931359.RAI-r5xR3z04A7LBbw9e7LaLaumCX6Dw1PVXAzdZq1qM0130_assertion description "[Spinocerebellar ataxia type 1 (SCA1) is an adult-onset, dominantly inherited neurodegenerative disease caused by expansion of a glutamine repeat tract in ataxin-1 (ATXN1).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP931359.RAI-r5xR3z04A7LBbw9e7LaLaumCX6Dw1PVXAzdZq1qM0130_provenance.