Matches in Nanopublications for { ?s ?p "[Alexander disease (AxD) is a rare neurodegenerative disorder characterized pathologically by the presence of eosinophilic inclusions known as Rosenthal fibers (RFs) within astrocytes, and is caused by dominant mutations in the coding region of the gene encoding glial fibrillary acidic protein (GFAP).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ?g. }
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- NP423201.RAX53aB8J7gCdNXlAF4WP9soXiuImZu1-wY6Iee0Uy5Ko130_assertion description "[Alexander disease (AxD) is a rare neurodegenerative disorder characterized pathologically by the presence of eosinophilic inclusions known as Rosenthal fibers (RFs) within astrocytes, and is caused by dominant mutations in the coding region of the gene encoding glial fibrillary acidic protein (GFAP).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP423201.RAX53aB8J7gCdNXlAF4WP9soXiuImZu1-wY6Iee0Uy5Ko130_provenance.
- NP1180372.RAKZTPKKf4T_R773T2JwXYdrOAnNNlkTt-ZwSU6e3siI4130_assertion description "[Alexander disease (AxD) is a rare neurodegenerative disorder characterized pathologically by the presence of eosinophilic inclusions known as Rosenthal fibers (RFs) within astrocytes, and is caused by dominant mutations in the coding region of the gene encoding glial fibrillary acidic protein (GFAP).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1180372.RAKZTPKKf4T_R773T2JwXYdrOAnNNlkTt-ZwSU6e3siI4130_provenance.