Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP315612.RAduEszkM3TMnGwUR2kOl4eZzKDteB7G0S71McALYb7OY130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP315612.RAduEszkM3TMnGwUR2kOl4eZzKDteB7G0S71McALYb7OY130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP315612.RAduEszkM3TMnGwUR2kOl4eZzKDteB7G0S71McALYb7OY130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP315612.RAduEszkM3TMnGwUR2kOl4eZzKDteB7G0S71McALYb7OY130_provenance.
- NP315612.RAduEszkM3TMnGwUR2kOl4eZzKDteB7G0S71McALYb7OY130_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." NP315612.RAduEszkM3TMnGwUR2kOl4eZzKDteB7G0S71McALYb7OY130_provenance.
- NP315612.RAduEszkM3TMnGwUR2kOl4eZzKDteB7G0S71McALYb7OY130_assertion evidence source_evidence_literature NP315612.RAduEszkM3TMnGwUR2kOl4eZzKDteB7G0S71McALYb7OY130_provenance.
- NP315612.RAduEszkM3TMnGwUR2kOl4eZzKDteB7G0S71McALYb7OY130_assertion SIO_000772 21297263 NP315612.RAduEszkM3TMnGwUR2kOl4eZzKDteB7G0S71McALYb7OY130_provenance.
- NP315612.RAduEszkM3TMnGwUR2kOl4eZzKDteB7G0S71McALYb7OY130_assertion wasDerivedFrom befree-20150227 NP315612.RAduEszkM3TMnGwUR2kOl4eZzKDteB7G0S71McALYb7OY130_provenance.
- NP315612.RAduEszkM3TMnGwUR2kOl4eZzKDteB7G0S71McALYb7OY130_assertion wasGeneratedBy ECO_0000203 NP315612.RAduEszkM3TMnGwUR2kOl4eZzKDteB7G0S71McALYb7OY130_provenance.
- befree-20150227 importedOn "2015-02-27" NP315612.RAduEszkM3TMnGwUR2kOl4eZzKDteB7G0S71McALYb7OY130_provenance.