Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP1249380.RAPE4dyY3FBeHWC4iIiWgjUTfdiAGaQZm9FIcDqHXBKjU130_assertion> ?p ?o ?g. }
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- NP1249380.RAPE4dyY3FBeHWC4iIiWgjUTfdiAGaQZm9FIcDqHXBKjU130_assertion type Assertion NP1249380.RAPE4dyY3FBeHWC4iIiWgjUTfdiAGaQZm9FIcDqHXBKjU130_head.
- NP1249380.RAPE4dyY3FBeHWC4iIiWgjUTfdiAGaQZm9FIcDqHXBKjU130_assertion description "[A number of rare mutations linked to familial AD (FAD) on the A? precursor protein (APP), Presenilin-1 (PS1), Presenilin- 2 (PS2), Adamalysin10, and other genetic risk factors for sporadic AD such as the ?4 allele of Apolipoprotein E (ApoE-?4) foster the accumulation of A? and also induce the entire spectrum of pathology associated with the disease.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1249380.RAPE4dyY3FBeHWC4iIiWgjUTfdiAGaQZm9FIcDqHXBKjU130_provenance.
- NP1249380.RAPE4dyY3FBeHWC4iIiWgjUTfdiAGaQZm9FIcDqHXBKjU130_assertion evidence source_evidence_literature NP1249380.RAPE4dyY3FBeHWC4iIiWgjUTfdiAGaQZm9FIcDqHXBKjU130_provenance.
- NP1249380.RAPE4dyY3FBeHWC4iIiWgjUTfdiAGaQZm9FIcDqHXBKjU130_assertion SIO_000772 25523424 NP1249380.RAPE4dyY3FBeHWC4iIiWgjUTfdiAGaQZm9FIcDqHXBKjU130_provenance.
- NP1249380.RAPE4dyY3FBeHWC4iIiWgjUTfdiAGaQZm9FIcDqHXBKjU130_assertion wasDerivedFrom befree-2016 NP1249380.RAPE4dyY3FBeHWC4iIiWgjUTfdiAGaQZm9FIcDqHXBKjU130_provenance.
- NP1249380.RAPE4dyY3FBeHWC4iIiWgjUTfdiAGaQZm9FIcDqHXBKjU130_assertion wasGeneratedBy ECO_0000203 NP1249380.RAPE4dyY3FBeHWC4iIiWgjUTfdiAGaQZm9FIcDqHXBKjU130_provenance.