Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP133373.RAYI2Zu1c1lGtfI2a8hRg53jxIP5F5Sw2eVuDbrtA8SEs130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP133373.RAYI2Zu1c1lGtfI2a8hRg53jxIP5F5Sw2eVuDbrtA8SEs130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP133373.RAYI2Zu1c1lGtfI2a8hRg53jxIP5F5Sw2eVuDbrtA8SEs130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the 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.
- NP133373.RAYI2Zu1c1lGtfI2a8hRg53jxIP5F5Sw2eVuDbrtA8SEs130_assertion evidence source_evidence_literature NP133373.RAYI2Zu1c1lGtfI2a8hRg53jxIP5F5Sw2eVuDbrtA8SEs130_provenance.
- NP133373.RAYI2Zu1c1lGtfI2a8hRg53jxIP5F5Sw2eVuDbrtA8SEs130_assertion SIO_000772 20697050 NP133373.RAYI2Zu1c1lGtfI2a8hRg53jxIP5F5Sw2eVuDbrtA8SEs130_provenance.
- NP133373.RAYI2Zu1c1lGtfI2a8hRg53jxIP5F5Sw2eVuDbrtA8SEs130_assertion wasDerivedFrom gad-20150221 NP133373.RAYI2Zu1c1lGtfI2a8hRg53jxIP5F5Sw2eVuDbrtA8SEs130_provenance.
- NP133373.RAYI2Zu1c1lGtfI2a8hRg53jxIP5F5Sw2eVuDbrtA8SEs130_assertion wasGeneratedBy ECO_0000203 NP133373.RAYI2Zu1c1lGtfI2a8hRg53jxIP5F5Sw2eVuDbrtA8SEs130_provenance.
- gad-20150221 importedOn "2015-02-21" NP133373.RAYI2Zu1c1lGtfI2a8hRg53jxIP5F5Sw2eVuDbrtA8SEs130_provenance.