Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP333602.RAzcvDLTkT8lYrLAUli1aZ_4yM1S7Sdc-jEWmMoomQCmM130_assertion> ?p ?o ?g. }
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- NP333602.RAzcvDLTkT8lYrLAUli1aZ_4yM1S7Sdc-jEWmMoomQCmM130_assertion type Assertion NP333602.RAzcvDLTkT8lYrLAUli1aZ_4yM1S7Sdc-jEWmMoomQCmM130_head.
- NP333602.RAzcvDLTkT8lYrLAUli1aZ_4yM1S7Sdc-jEWmMoomQCmM130_assertion wasGeneratedBy ECO_0000203 NP333602.RAzcvDLTkT8lYrLAUli1aZ_4yM1S7Sdc-jEWmMoomQCmM130_provenance.
- NP333602.RAzcvDLTkT8lYrLAUli1aZ_4yM1S7Sdc-jEWmMoomQCmM130_assertion wasDerivedFrom befree-20150227 NP333602.RAzcvDLTkT8lYrLAUli1aZ_4yM1S7Sdc-jEWmMoomQCmM130_provenance.
- NP333602.RAzcvDLTkT8lYrLAUli1aZ_4yM1S7Sdc-jEWmMoomQCmM130_assertion SIO_000772 12146803 NP333602.RAzcvDLTkT8lYrLAUli1aZ_4yM1S7Sdc-jEWmMoomQCmM130_provenance.
- NP333602.RAzcvDLTkT8lYrLAUli1aZ_4yM1S7Sdc-jEWmMoomQCmM130_assertion evidence source_evidence_literature NP333602.RAzcvDLTkT8lYrLAUli1aZ_4yM1S7Sdc-jEWmMoomQCmM130_provenance.
- NP333602.RAzcvDLTkT8lYrLAUli1aZ_4yM1S7Sdc-jEWmMoomQCmM130_assertion description "[CAA occurs in several familial conditions, including hereditary cerebral hemorrhage with amyloidosis of Icelandic type caused by deposition of mutant cystatin C, hereditary cerebral hemorrhage with amyloidosis Dutch type and familial AD with deposition of either A beta variants or wild-type A beta, the transthyretin-related meningo-vascular amyloidoses, gelsolin as well as familial prion disease-related CAAs and the recently described BRI2 gene-related CAAs in familial British dementia and familial Danish dementia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP333602.RAzcvDLTkT8lYrLAUli1aZ_4yM1S7Sdc-jEWmMoomQCmM130_provenance.