Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP777297.RA2w-VeHQe5Tmh6shulx5I6SlKen_7QKBoV5LTC4T5mSg130_assertion> ?p ?o ?g. }
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- NP777297.RA2w-VeHQe5Tmh6shulx5I6SlKen_7QKBoV5LTC4T5mSg130_assertion type Assertion NP777297.RA2w-VeHQe5Tmh6shulx5I6SlKen_7QKBoV5LTC4T5mSg130_head.
- NP777297.RA2w-VeHQe5Tmh6shulx5I6SlKen_7QKBoV5LTC4T5mSg130_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." NP777297.RA2w-VeHQe5Tmh6shulx5I6SlKen_7QKBoV5LTC4T5mSg130_provenance.
- NP777297.RA2w-VeHQe5Tmh6shulx5I6SlKen_7QKBoV5LTC4T5mSg130_assertion evidence source_evidence_literature NP777297.RA2w-VeHQe5Tmh6shulx5I6SlKen_7QKBoV5LTC4T5mSg130_provenance.
- NP777297.RA2w-VeHQe5Tmh6shulx5I6SlKen_7QKBoV5LTC4T5mSg130_assertion SIO_000772 19933183 NP777297.RA2w-VeHQe5Tmh6shulx5I6SlKen_7QKBoV5LTC4T5mSg130_provenance.
- NP777297.RA2w-VeHQe5Tmh6shulx5I6SlKen_7QKBoV5LTC4T5mSg130_assertion wasDerivedFrom befree-2016 NP777297.RA2w-VeHQe5Tmh6shulx5I6SlKen_7QKBoV5LTC4T5mSg130_provenance.
- NP777297.RA2w-VeHQe5Tmh6shulx5I6SlKen_7QKBoV5LTC4T5mSg130_assertion wasGeneratedBy ECO_0000203 NP777297.RA2w-VeHQe5Tmh6shulx5I6SlKen_7QKBoV5LTC4T5mSg130_provenance.