Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP777296.RASBzBoFUWn6Xbx1qwiVd2fqoUkcQhrjDupGvToEU-kb8130_assertion> ?p ?o ?g. }
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- NP777296.RASBzBoFUWn6Xbx1qwiVd2fqoUkcQhrjDupGvToEU-kb8130_assertion type Assertion NP777296.RASBzBoFUWn6Xbx1qwiVd2fqoUkcQhrjDupGvToEU-kb8130_head.
- NP777296.RASBzBoFUWn6Xbx1qwiVd2fqoUkcQhrjDupGvToEU-kb8130_assertion description "[In this study, NR2E3 mutations (p.G56R, p.V118M) were found to be responsible for approximately 2.9% of overall RP in Chinese patients, comparable to the contributions of RHO and RP1 mutations.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP777296.RASBzBoFUWn6Xbx1qwiVd2fqoUkcQhrjDupGvToEU-kb8130_provenance.
- NP777296.RASBzBoFUWn6Xbx1qwiVd2fqoUkcQhrjDupGvToEU-kb8130_assertion evidence source_evidence_literature NP777296.RASBzBoFUWn6Xbx1qwiVd2fqoUkcQhrjDupGvToEU-kb8130_provenance.
- NP777296.RASBzBoFUWn6Xbx1qwiVd2fqoUkcQhrjDupGvToEU-kb8130_assertion SIO_000772 19933183 NP777296.RASBzBoFUWn6Xbx1qwiVd2fqoUkcQhrjDupGvToEU-kb8130_provenance.
- NP777296.RASBzBoFUWn6Xbx1qwiVd2fqoUkcQhrjDupGvToEU-kb8130_assertion wasDerivedFrom befree-2016 NP777296.RASBzBoFUWn6Xbx1qwiVd2fqoUkcQhrjDupGvToEU-kb8130_provenance.
- NP777296.RASBzBoFUWn6Xbx1qwiVd2fqoUkcQhrjDupGvToEU-kb8130_assertion wasGeneratedBy ECO_0000203 NP777296.RASBzBoFUWn6Xbx1qwiVd2fqoUkcQhrjDupGvToEU-kb8130_provenance.