Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP695662.RAhv1SnAXG9Y6c4_t_AwLWtz33e-OQRIxKAEf2cF_XW-g130_assertion> ?p ?o ?g. }
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- NP695662.RAhv1SnAXG9Y6c4_t_AwLWtz33e-OQRIxKAEf2cF_XW-g130_assertion type Assertion NP695662.RAhv1SnAXG9Y6c4_t_AwLWtz33e-OQRIxKAEf2cF_XW-g130_head.
- NP695662.RAhv1SnAXG9Y6c4_t_AwLWtz33e-OQRIxKAEf2cF_XW-g130_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." NP695662.RAhv1SnAXG9Y6c4_t_AwLWtz33e-OQRIxKAEf2cF_XW-g130_provenance.
- NP695662.RAhv1SnAXG9Y6c4_t_AwLWtz33e-OQRIxKAEf2cF_XW-g130_assertion evidence source_evidence_literature NP695662.RAhv1SnAXG9Y6c4_t_AwLWtz33e-OQRIxKAEf2cF_XW-g130_provenance.
- NP695662.RAhv1SnAXG9Y6c4_t_AwLWtz33e-OQRIxKAEf2cF_XW-g130_assertion SIO_000772 19933183 NP695662.RAhv1SnAXG9Y6c4_t_AwLWtz33e-OQRIxKAEf2cF_XW-g130_provenance.
- NP695662.RAhv1SnAXG9Y6c4_t_AwLWtz33e-OQRIxKAEf2cF_XW-g130_assertion wasDerivedFrom befree-20140225 NP695662.RAhv1SnAXG9Y6c4_t_AwLWtz33e-OQRIxKAEf2cF_XW-g130_provenance.
- NP695662.RAhv1SnAXG9Y6c4_t_AwLWtz33e-OQRIxKAEf2cF_XW-g130_assertion wasGeneratedBy ECO_0000203 NP695662.RAhv1SnAXG9Y6c4_t_AwLWtz33e-OQRIxKAEf2cF_XW-g130_provenance.