Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP677920.RACCn3F-ycTDsPTs8su_ep-U98v1cQhGIdBkxg8_JCLQ4130_assertion> ?p ?o ?g. }
Showing items 1 to 6 of
6
with 100 items per page.
- NP677920.RACCn3F-ycTDsPTs8su_ep-U98v1cQhGIdBkxg8_JCLQ4130_assertion type Assertion NP677920.RACCn3F-ycTDsPTs8su_ep-U98v1cQhGIdBkxg8_JCLQ4130_head.
- NP677920.RACCn3F-ycTDsPTs8su_ep-U98v1cQhGIdBkxg8_JCLQ4130_assertion description "[CNS involvement is rare in systemic amyloidoses due to transthyretin (TTR) mutation and manifests as a combination of dementia, seizures, and myelopathy.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP677920.RACCn3F-ycTDsPTs8su_ep-U98v1cQhGIdBkxg8_JCLQ4130_provenance.
- NP677920.RACCn3F-ycTDsPTs8su_ep-U98v1cQhGIdBkxg8_JCLQ4130_assertion evidence source_evidence_literature NP677920.RACCn3F-ycTDsPTs8su_ep-U98v1cQhGIdBkxg8_JCLQ4130_provenance.
- NP677920.RACCn3F-ycTDsPTs8su_ep-U98v1cQhGIdBkxg8_JCLQ4130_assertion SIO_000772 11445644 NP677920.RACCn3F-ycTDsPTs8su_ep-U98v1cQhGIdBkxg8_JCLQ4130_provenance.
- NP677920.RACCn3F-ycTDsPTs8su_ep-U98v1cQhGIdBkxg8_JCLQ4130_assertion wasDerivedFrom befree-20140225 NP677920.RACCn3F-ycTDsPTs8su_ep-U98v1cQhGIdBkxg8_JCLQ4130_provenance.
- NP677920.RACCn3F-ycTDsPTs8su_ep-U98v1cQhGIdBkxg8_JCLQ4130_assertion wasGeneratedBy ECO_0000203 NP677920.RACCn3F-ycTDsPTs8su_ep-U98v1cQhGIdBkxg8_JCLQ4130_provenance.