Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP133374.RAb3P6khvNv7rmy6a-fuGJkL2JD6RRuoVl25GfReqJU-E130_assertion> ?p ?o ?g. }
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- NP133374.RAb3P6khvNv7rmy6a-fuGJkL2JD6RRuoVl25GfReqJU-E130_assertion type Assertion NP133374.RAb3P6khvNv7rmy6a-fuGJkL2JD6RRuoVl25GfReqJU-E130_head.
- NP133374.RAb3P6khvNv7rmy6a-fuGJkL2JD6RRuoVl25GfReqJU-E130_assertion wasGeneratedBy ECO_0000203 NP133374.RAb3P6khvNv7rmy6a-fuGJkL2JD6RRuoVl25GfReqJU-E130_provenance.
- NP133374.RAb3P6khvNv7rmy6a-fuGJkL2JD6RRuoVl25GfReqJU-E130_assertion wasDerivedFrom gad-20150221 NP133374.RAb3P6khvNv7rmy6a-fuGJkL2JD6RRuoVl25GfReqJU-E130_provenance.
- NP133374.RAb3P6khvNv7rmy6a-fuGJkL2JD6RRuoVl25GfReqJU-E130_assertion SIO_000772 20697050 NP133374.RAb3P6khvNv7rmy6a-fuGJkL2JD6RRuoVl25GfReqJU-E130_provenance.
- NP133374.RAb3P6khvNv7rmy6a-fuGJkL2JD6RRuoVl25GfReqJU-E130_assertion evidence source_evidence_literature NP133374.RAb3P6khvNv7rmy6a-fuGJkL2JD6RRuoVl25GfReqJU-E130_provenance.
- NP133374.RAb3P6khvNv7rmy6a-fuGJkL2JD6RRuoVl25GfReqJU-E130_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." NP133374.RAb3P6khvNv7rmy6a-fuGJkL2JD6RRuoVl25GfReqJU-E130_provenance.