Matches in Nanopublications for { ?s ?p "[Missense mutations in the AFG3L2 proteolytic domain account for ?1.5% of European autosomal dominant cerebellar ataxias.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ?g. }
Showing items 1 to 4 of
4
with 100 items per page.
- assertion description "[Missense mutations in the AFG3L2 proteolytic domain account for ?1.5% of European autosomal dominant cerebellar ataxias.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
- assertion description "[Missense mutations in the AFG3L2 proteolytic domain account for ?1.5% of European autosomal dominant cerebellar ataxias.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
- NP856458.RAgzu2UfIT1Wm9j9RVmyYpOVVgb7br-9oZRgwz56TPptQ130_assertion description "[Missense mutations in the AFG3L2 proteolytic domain account for ?1.5% of European autosomal dominant cerebellar ataxias.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP856458.RAgzu2UfIT1Wm9j9RVmyYpOVVgb7br-9oZRgwz56TPptQ130_provenance.
- NP834004.RAQiBu5HZv2bWrkxKiApz5wTxRAIRw_tGeU0lSWzkCaNs130_assertion description "[Missense mutations in the AFG3L2 proteolytic domain account for ?1.5% of European autosomal dominant cerebellar ataxias.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP834004.RAQiBu5HZv2bWrkxKiApz5wTxRAIRw_tGeU0lSWzkCaNs130_provenance.