Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP556116.RAa6xgsSm40R-9LRxy3BnLUg0t1PaZp2PhUOXOSGl7HHI130_assertion> ?p ?o ?g. }
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- NP556116.RAa6xgsSm40R-9LRxy3BnLUg0t1PaZp2PhUOXOSGl7HHI130_assertion type Assertion NP556116.RAa6xgsSm40R-9LRxy3BnLUg0t1PaZp2PhUOXOSGl7HHI130_head.
- 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.