Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP665036.RA7imWzN93rUBeQt7RoHAWyQfxkJPP8m6NAI5UQr5GNnU130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP665036.RA7imWzN93rUBeQt7RoHAWyQfxkJPP8m6NAI5UQr5GNnU130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP665036.RA7imWzN93rUBeQt7RoHAWyQfxkJPP8m6NAI5UQr5GNnU130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP665036.RA7imWzN93rUBeQt7RoHAWyQfxkJPP8m6NAI5UQr5GNnU130_provenance.
- befree-2016 importedOn "2016-02-19" NP665036.RA7imWzN93rUBeQt7RoHAWyQfxkJPP8m6NAI5UQr5GNnU130_provenance.
- NP665036.RA7imWzN93rUBeQt7RoHAWyQfxkJPP8m6NAI5UQr5GNnU130_assertion wasGeneratedBy ECO_0000203 NP665036.RA7imWzN93rUBeQt7RoHAWyQfxkJPP8m6NAI5UQr5GNnU130_provenance.
- NP665036.RA7imWzN93rUBeQt7RoHAWyQfxkJPP8m6NAI5UQr5GNnU130_assertion wasDerivedFrom befree-2016 NP665036.RA7imWzN93rUBeQt7RoHAWyQfxkJPP8m6NAI5UQr5GNnU130_provenance.
- NP665036.RA7imWzN93rUBeQt7RoHAWyQfxkJPP8m6NAI5UQr5GNnU130_assertion SIO_000772 18401171 NP665036.RA7imWzN93rUBeQt7RoHAWyQfxkJPP8m6NAI5UQr5GNnU130_provenance.
- NP665036.RA7imWzN93rUBeQt7RoHAWyQfxkJPP8m6NAI5UQr5GNnU130_assertion evidence source_evidence_literature NP665036.RA7imWzN93rUBeQt7RoHAWyQfxkJPP8m6NAI5UQr5GNnU130_provenance.
- NP665036.RA7imWzN93rUBeQt7RoHAWyQfxkJPP8m6NAI5UQr5GNnU130_assertion description "[This finding is of great clinical importance as nondemented patients positive for APOE epsilon4 could be identified as being at genetic risk of AD, and for that reason monitored more closely.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP665036.RA7imWzN93rUBeQt7RoHAWyQfxkJPP8m6NAI5UQr5GNnU130_provenance.