Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP415973.RALNxwBr88na8hE1oXqjWLrPpogXvQFODKCPdEl0-XQqo130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP415973.RALNxwBr88na8hE1oXqjWLrPpogXvQFODKCPdEl0-XQqo130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP415973.RALNxwBr88na8hE1oXqjWLrPpogXvQFODKCPdEl0-XQqo130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP415973.RALNxwBr88na8hE1oXqjWLrPpogXvQFODKCPdEl0-XQqo130_provenance.
- NP415973.RALNxwBr88na8hE1oXqjWLrPpogXvQFODKCPdEl0-XQqo130_assertion description "[The associated region extends 120 kb encompassing 11 candidate genes.While AGER encodes a key receptor for amyloid-? protein, an analysis of network context based upon genes now confirmed to contribute to dementia risk (A?PP, PSEN1, PSEN2, CR1, CLU, PICALM, and APOE) suggested strong functional coupling to NOTCH4, with no significant coupling to the remaining candidates.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP415973.RALNxwBr88na8hE1oXqjWLrPpogXvQFODKCPdEl0-XQqo130_provenance.
- NP415973.RALNxwBr88na8hE1oXqjWLrPpogXvQFODKCPdEl0-XQqo130_assertion evidence source_evidence_literature NP415973.RALNxwBr88na8hE1oXqjWLrPpogXvQFODKCPdEl0-XQqo130_provenance.
- NP415973.RALNxwBr88na8hE1oXqjWLrPpogXvQFODKCPdEl0-XQqo130_assertion SIO_000772 21297263 NP415973.RALNxwBr88na8hE1oXqjWLrPpogXvQFODKCPdEl0-XQqo130_provenance.
- NP415973.RALNxwBr88na8hE1oXqjWLrPpogXvQFODKCPdEl0-XQqo130_assertion wasDerivedFrom befree-20140225 NP415973.RALNxwBr88na8hE1oXqjWLrPpogXvQFODKCPdEl0-XQqo130_provenance.
- NP415973.RALNxwBr88na8hE1oXqjWLrPpogXvQFODKCPdEl0-XQqo130_assertion wasGeneratedBy ECO_0000203 NP415973.RALNxwBr88na8hE1oXqjWLrPpogXvQFODKCPdEl0-XQqo130_provenance.
- befree-20140225 importedOn "2014-02-25" NP415973.RALNxwBr88na8hE1oXqjWLrPpogXvQFODKCPdEl0-XQqo130_provenance.