Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP1249377.RA-GS8JiqgU4EyZDykD2cCm6tlj9UrIdvnBmWj6_iqOgY130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP1249377.RA-GS8JiqgU4EyZDykD2cCm6tlj9UrIdvnBmWj6_iqOgY130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP1249377.RA-GS8JiqgU4EyZDykD2cCm6tlj9UrIdvnBmWj6_iqOgY130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP1249377.RA-GS8JiqgU4EyZDykD2cCm6tlj9UrIdvnBmWj6_iqOgY130_provenance.
- NP1249377.RA-GS8JiqgU4EyZDykD2cCm6tlj9UrIdvnBmWj6_iqOgY130_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." NP1249377.RA-GS8JiqgU4EyZDykD2cCm6tlj9UrIdvnBmWj6_iqOgY130_provenance.
- NP1249377.RA-GS8JiqgU4EyZDykD2cCm6tlj9UrIdvnBmWj6_iqOgY130_assertion evidence source_evidence_literature NP1249377.RA-GS8JiqgU4EyZDykD2cCm6tlj9UrIdvnBmWj6_iqOgY130_provenance.
- NP1249377.RA-GS8JiqgU4EyZDykD2cCm6tlj9UrIdvnBmWj6_iqOgY130_assertion SIO_000772 25523424 NP1249377.RA-GS8JiqgU4EyZDykD2cCm6tlj9UrIdvnBmWj6_iqOgY130_provenance.
- NP1249377.RA-GS8JiqgU4EyZDykD2cCm6tlj9UrIdvnBmWj6_iqOgY130_assertion wasDerivedFrom befree-2016 NP1249377.RA-GS8JiqgU4EyZDykD2cCm6tlj9UrIdvnBmWj6_iqOgY130_provenance.
- NP1249377.RA-GS8JiqgU4EyZDykD2cCm6tlj9UrIdvnBmWj6_iqOgY130_assertion wasGeneratedBy ECO_0000203 NP1249377.RA-GS8JiqgU4EyZDykD2cCm6tlj9UrIdvnBmWj6_iqOgY130_provenance.
- befree-2016 importedOn "2016-02-19" NP1249377.RA-GS8JiqgU4EyZDykD2cCm6tlj9UrIdvnBmWj6_iqOgY130_provenance.