Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP677920.RACCn3F-ycTDsPTs8su_ep-U98v1cQhGIdBkxg8_JCLQ4130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP677920.RACCn3F-ycTDsPTs8su_ep-U98v1cQhGIdBkxg8_JCLQ4130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP677920.RACCn3F-ycTDsPTs8su_ep-U98v1cQhGIdBkxg8_JCLQ4130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP677920.RACCn3F-ycTDsPTs8su_ep-U98v1cQhGIdBkxg8_JCLQ4130_provenance.
- 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.
- befree-20140225 importedOn "2014-02-25" NP677920.RACCn3F-ycTDsPTs8su_ep-U98v1cQhGIdBkxg8_JCLQ4130_provenance.