Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP777296.RASBzBoFUWn6Xbx1qwiVd2fqoUkcQhrjDupGvToEU-kb8130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP777296.RASBzBoFUWn6Xbx1qwiVd2fqoUkcQhrjDupGvToEU-kb8130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP777296.RASBzBoFUWn6Xbx1qwiVd2fqoUkcQhrjDupGvToEU-kb8130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP777296.RASBzBoFUWn6Xbx1qwiVd2fqoUkcQhrjDupGvToEU-kb8130_provenance.
- 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.
- befree-2016 importedOn "2016-02-19" NP777296.RASBzBoFUWn6Xbx1qwiVd2fqoUkcQhrjDupGvToEU-kb8130_provenance.