Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP497074.RAKeNsH0IEb-h6S2e7wBzxOzTsjY85YOguckJ_drwjhFM130_assertion> ?p ?o ?g. }
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- NP497074.RAKeNsH0IEb-h6S2e7wBzxOzTsjY85YOguckJ_drwjhFM130_assertion type Assertion NP497074.RAKeNsH0IEb-h6S2e7wBzxOzTsjY85YOguckJ_drwjhFM130_head.
- NP497074.RAKeNsH0IEb-h6S2e7wBzxOzTsjY85YOguckJ_drwjhFM130_assertion description "[We also tested for the APP codon 693 mutation associated with hereditary cerebral hemorrhage with amyloidosis-Dutch type, for PRIP gene missense mutations at codons 102, 117, and 200, and for the PRIP insertion mutations which are associated with Creutzfeld-Jakob disease and Gerstmann-Straussler Scheinker syndrome.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP497074.RAKeNsH0IEb-h6S2e7wBzxOzTsjY85YOguckJ_drwjhFM130_provenance.
- NP497074.RAKeNsH0IEb-h6S2e7wBzxOzTsjY85YOguckJ_drwjhFM130_assertion evidence source_evidence_literature NP497074.RAKeNsH0IEb-h6S2e7wBzxOzTsjY85YOguckJ_drwjhFM130_provenance.
- NP497074.RAKeNsH0IEb-h6S2e7wBzxOzTsjY85YOguckJ_drwjhFM130_assertion SIO_000772 1679288 NP497074.RAKeNsH0IEb-h6S2e7wBzxOzTsjY85YOguckJ_drwjhFM130_provenance.
- NP497074.RAKeNsH0IEb-h6S2e7wBzxOzTsjY85YOguckJ_drwjhFM130_assertion wasDerivedFrom befree-20140225 NP497074.RAKeNsH0IEb-h6S2e7wBzxOzTsjY85YOguckJ_drwjhFM130_provenance.
- NP497074.RAKeNsH0IEb-h6S2e7wBzxOzTsjY85YOguckJ_drwjhFM130_assertion wasGeneratedBy ECO_0000203 NP497074.RAKeNsH0IEb-h6S2e7wBzxOzTsjY85YOguckJ_drwjhFM130_provenance.