Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP1380076.RArmYyYk2sJViqGIjT5PPewZd5MLX8WDkr68Y-SHf5Glk130_assertion> ?p ?o ?g. }
Showing items 1 to 6 of
6
with 100 items per page.
- NP1380076.RArmYyYk2sJViqGIjT5PPewZd5MLX8WDkr68Y-SHf5Glk130_assertion type Assertion NP1380076.RArmYyYk2sJViqGIjT5PPewZd5MLX8WDkr68Y-SHf5Glk130_head.
- NP1380076.RArmYyYk2sJViqGIjT5PPewZd5MLX8WDkr68Y-SHf5Glk130_assertion description "[We investigated the allelic origin of PrP(res) in brains of subjects heterozygous for the D178N mutation linked to fatal familial insomnia (FFI) and a subtype of Creutzfeldt-Jakob disease (CJD178), as well as for insertional mutations associated with another CJD subtype.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1380076.RArmYyYk2sJViqGIjT5PPewZd5MLX8WDkr68Y-SHf5Glk130_provenance.
- NP1380076.RArmYyYk2sJViqGIjT5PPewZd5MLX8WDkr68Y-SHf5Glk130_assertion evidence source_evidence_literature NP1380076.RArmYyYk2sJViqGIjT5PPewZd5MLX8WDkr68Y-SHf5Glk130_provenance.
- NP1380076.RArmYyYk2sJViqGIjT5PPewZd5MLX8WDkr68Y-SHf5Glk130_assertion SIO_000772 9288728 NP1380076.RArmYyYk2sJViqGIjT5PPewZd5MLX8WDkr68Y-SHf5Glk130_provenance.
- NP1380076.RArmYyYk2sJViqGIjT5PPewZd5MLX8WDkr68Y-SHf5Glk130_assertion wasDerivedFrom befree-2016 NP1380076.RArmYyYk2sJViqGIjT5PPewZd5MLX8WDkr68Y-SHf5Glk130_provenance.
- NP1380076.RArmYyYk2sJViqGIjT5PPewZd5MLX8WDkr68Y-SHf5Glk130_assertion wasGeneratedBy ECO_0000203 NP1380076.RArmYyYk2sJViqGIjT5PPewZd5MLX8WDkr68Y-SHf5Glk130_provenance.