Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP423201.RAX53aB8J7gCdNXlAF4WP9soXiuImZu1-wY6Iee0Uy5Ko130_assertion> ?p ?o ?g. }
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- NP423201.RAX53aB8J7gCdNXlAF4WP9soXiuImZu1-wY6Iee0Uy5Ko130_assertion type Assertion NP423201.RAX53aB8J7gCdNXlAF4WP9soXiuImZu1-wY6Iee0Uy5Ko130_head.
- 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.
- NP423201.RAX53aB8J7gCdNXlAF4WP9soXiuImZu1-wY6Iee0Uy5Ko130_assertion evidence source_evidence_literature NP423201.RAX53aB8J7gCdNXlAF4WP9soXiuImZu1-wY6Iee0Uy5Ko130_provenance.
- NP423201.RAX53aB8J7gCdNXlAF4WP9soXiuImZu1-wY6Iee0Uy5Ko130_assertion SIO_000772 24806671 NP423201.RAX53aB8J7gCdNXlAF4WP9soXiuImZu1-wY6Iee0Uy5Ko130_provenance.
- NP423201.RAX53aB8J7gCdNXlAF4WP9soXiuImZu1-wY6Iee0Uy5Ko130_assertion wasDerivedFrom befree-20150227 NP423201.RAX53aB8J7gCdNXlAF4WP9soXiuImZu1-wY6Iee0Uy5Ko130_provenance.
- NP423201.RAX53aB8J7gCdNXlAF4WP9soXiuImZu1-wY6Iee0Uy5Ko130_assertion wasGeneratedBy ECO_0000203 NP423201.RAX53aB8J7gCdNXlAF4WP9soXiuImZu1-wY6Iee0Uy5Ko130_provenance.