Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP133373.RAYI2Zu1c1lGtfI2a8hRg53jxIP5F5Sw2eVuDbrtA8SEs130_assertion> ?p ?o ?g. }
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- NP133373.RAYI2Zu1c1lGtfI2a8hRg53jxIP5F5Sw2eVuDbrtA8SEs130_assertion type Assertion NP133373.RAYI2Zu1c1lGtfI2a8hRg53jxIP5F5Sw2eVuDbrtA8SEs130_head.
- NP133373.RAYI2Zu1c1lGtfI2a8hRg53jxIP5F5Sw2eVuDbrtA8SEs130_assertion wasGeneratedBy ECO_0000203 NP133373.RAYI2Zu1c1lGtfI2a8hRg53jxIP5F5Sw2eVuDbrtA8SEs130_provenance.
- NP133373.RAYI2Zu1c1lGtfI2a8hRg53jxIP5F5Sw2eVuDbrtA8SEs130_assertion wasDerivedFrom gad-20150221 NP133373.RAYI2Zu1c1lGtfI2a8hRg53jxIP5F5Sw2eVuDbrtA8SEs130_provenance.
- NP133373.RAYI2Zu1c1lGtfI2a8hRg53jxIP5F5Sw2eVuDbrtA8SEs130_assertion SIO_000772 20697050 NP133373.RAYI2Zu1c1lGtfI2a8hRg53jxIP5F5Sw2eVuDbrtA8SEs130_provenance.
- NP133373.RAYI2Zu1c1lGtfI2a8hRg53jxIP5F5Sw2eVuDbrtA8SEs130_assertion evidence source_evidence_literature NP133373.RAYI2Zu1c1lGtfI2a8hRg53jxIP5F5Sw2eVuDbrtA8SEs130_provenance.
- NP133373.RAYI2Zu1c1lGtfI2a8hRg53jxIP5F5Sw2eVuDbrtA8SEs130_assertion description "[These findings expand the number of APP mutations linked to hereditary cerebral hemorrhage with amyloidosis, reinforcing the link between this phenotype and codon 693 of APP.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP133373.RAYI2Zu1c1lGtfI2a8hRg53jxIP5F5Sw2eVuDbrtA8SEs130_provenance.