Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP556116.RAa6xgsSm40R-9LRxy3BnLUg0t1PaZp2PhUOXOSGl7HHI130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP556116.RAa6xgsSm40R-9LRxy3BnLUg0t1PaZp2PhUOXOSGl7HHI130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP556116.RAa6xgsSm40R-9LRxy3BnLUg0t1PaZp2PhUOXOSGl7HHI130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP556116.RAa6xgsSm40R-9LRxy3BnLUg0t1PaZp2PhUOXOSGl7HHI130_provenance.
- NP556116.RAa6xgsSm40R-9LRxy3BnLUg0t1PaZp2PhUOXOSGl7HHI130_assertion description "[APP717, APP693, and PRIP gene mutations are rare in Alzheimer disease.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP556116.RAa6xgsSm40R-9LRxy3BnLUg0t1PaZp2PhUOXOSGl7HHI130_provenance.
- NP556116.RAa6xgsSm40R-9LRxy3BnLUg0t1PaZp2PhUOXOSGl7HHI130_assertion evidence source_evidence_literature NP556116.RAa6xgsSm40R-9LRxy3BnLUg0t1PaZp2PhUOXOSGl7HHI130_provenance.
- NP556116.RAa6xgsSm40R-9LRxy3BnLUg0t1PaZp2PhUOXOSGl7HHI130_assertion SIO_000772 1679288 NP556116.RAa6xgsSm40R-9LRxy3BnLUg0t1PaZp2PhUOXOSGl7HHI130_provenance.
- NP556116.RAa6xgsSm40R-9LRxy3BnLUg0t1PaZp2PhUOXOSGl7HHI130_assertion wasDerivedFrom befree-2016 NP556116.RAa6xgsSm40R-9LRxy3BnLUg0t1PaZp2PhUOXOSGl7HHI130_provenance.
- NP556116.RAa6xgsSm40R-9LRxy3BnLUg0t1PaZp2PhUOXOSGl7HHI130_assertion wasGeneratedBy ECO_0000203 NP556116.RAa6xgsSm40R-9LRxy3BnLUg0t1PaZp2PhUOXOSGl7HHI130_provenance.
- befree-2016 importedOn "2016-02-19" NP556116.RAa6xgsSm40R-9LRxy3BnLUg0t1PaZp2PhUOXOSGl7HHI130_provenance.