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- NP672006.RAh47guzhwJvHBmpESlnJ9YpJL71HPfpvCm2zXII26NTA130_assertion type Assertion NP672006.RAh47guzhwJvHBmpESlnJ9YpJL71HPfpvCm2zXII26NTA130_head.
- NP672006.RAh47guzhwJvHBmpESlnJ9YpJL71HPfpvCm2zXII26NTA130_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." NP672006.RAh47guzhwJvHBmpESlnJ9YpJL71HPfpvCm2zXII26NTA130_provenance.
- NP672006.RAh47guzhwJvHBmpESlnJ9YpJL71HPfpvCm2zXII26NTA130_assertion evidence source_evidence_literature NP672006.RAh47guzhwJvHBmpESlnJ9YpJL71HPfpvCm2zXII26NTA130_provenance.
- NP672006.RAh47guzhwJvHBmpESlnJ9YpJL71HPfpvCm2zXII26NTA130_assertion SIO_000772 19933183 NP672006.RAh47guzhwJvHBmpESlnJ9YpJL71HPfpvCm2zXII26NTA130_provenance.
- NP672006.RAh47guzhwJvHBmpESlnJ9YpJL71HPfpvCm2zXII26NTA130_assertion wasDerivedFrom befree-20150227 NP672006.RAh47guzhwJvHBmpESlnJ9YpJL71HPfpvCm2zXII26NTA130_provenance.
- NP672006.RAh47guzhwJvHBmpESlnJ9YpJL71HPfpvCm2zXII26NTA130_assertion wasGeneratedBy ECO_0000203 NP672006.RAh47guzhwJvHBmpESlnJ9YpJL71HPfpvCm2zXII26NTA130_provenance.