Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP262509.RA6iL_s4P3QVR0VpBoZL31dJpxudAi7eatNI1GZLOVlv8130_assertion> ?p ?o ?g. }
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- NP262509.RA6iL_s4P3QVR0VpBoZL31dJpxudAi7eatNI1GZLOVlv8130_assertion type Assertion NP262509.RA6iL_s4P3QVR0VpBoZL31dJpxudAi7eatNI1GZLOVlv8130_head.
- NP262509.RA6iL_s4P3QVR0VpBoZL31dJpxudAi7eatNI1GZLOVlv8130_assertion description "[This figure is comparable to the percentage of RP2 gene mutations that we have detected in our entire XLRP patient pool (10%-15%).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP262509.RA6iL_s4P3QVR0VpBoZL31dJpxudAi7eatNI1GZLOVlv8130_provenance.
- NP262509.RA6iL_s4P3QVR0VpBoZL31dJpxudAi7eatNI1GZLOVlv8130_assertion evidence source_evidence_literature NP262509.RA6iL_s4P3QVR0VpBoZL31dJpxudAi7eatNI1GZLOVlv8130_provenance.
- NP262509.RA6iL_s4P3QVR0VpBoZL31dJpxudAi7eatNI1GZLOVlv8130_assertion SIO_000772 10480356 NP262509.RA6iL_s4P3QVR0VpBoZL31dJpxudAi7eatNI1GZLOVlv8130_provenance.
- NP262509.RA6iL_s4P3QVR0VpBoZL31dJpxudAi7eatNI1GZLOVlv8130_assertion wasDerivedFrom befree-2016 NP262509.RA6iL_s4P3QVR0VpBoZL31dJpxudAi7eatNI1GZLOVlv8130_provenance.
- NP262509.RA6iL_s4P3QVR0VpBoZL31dJpxudAi7eatNI1GZLOVlv8130_assertion wasGeneratedBy ECO_0000203 NP262509.RA6iL_s4P3QVR0VpBoZL31dJpxudAi7eatNI1GZLOVlv8130_provenance.