Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP925520.RALqNuHjWV9lozrxRV_aNrHSrtSrmPGXVJLMTKic2cV7c130_assertion> ?p ?o ?g. }
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- NP925520.RALqNuHjWV9lozrxRV_aNrHSrtSrmPGXVJLMTKic2cV7c130_assertion type Assertion NP925520.RALqNuHjWV9lozrxRV_aNrHSrtSrmPGXVJLMTKic2cV7c130_head.
- NP925520.RALqNuHjWV9lozrxRV_aNrHSrtSrmPGXVJLMTKic2cV7c130_assertion description "[This study identified a novel disease-causing mutation p.R187C in MIP in a Chinese cataract family, expanding the mutation spectrum of MIP causing congenital cataract.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP925520.RALqNuHjWV9lozrxRV_aNrHSrtSrmPGXVJLMTKic2cV7c130_provenance.
- NP925520.RALqNuHjWV9lozrxRV_aNrHSrtSrmPGXVJLMTKic2cV7c130_assertion evidence source_evidence_literature NP925520.RALqNuHjWV9lozrxRV_aNrHSrtSrmPGXVJLMTKic2cV7c130_provenance.
- NP925520.RALqNuHjWV9lozrxRV_aNrHSrtSrmPGXVJLMTKic2cV7c130_assertion SIO_000772 21245956 NP925520.RALqNuHjWV9lozrxRV_aNrHSrtSrmPGXVJLMTKic2cV7c130_provenance.
- NP925520.RALqNuHjWV9lozrxRV_aNrHSrtSrmPGXVJLMTKic2cV7c130_assertion wasDerivedFrom befree-20140225 NP925520.RALqNuHjWV9lozrxRV_aNrHSrtSrmPGXVJLMTKic2cV7c130_provenance.
- NP925520.RALqNuHjWV9lozrxRV_aNrHSrtSrmPGXVJLMTKic2cV7c130_assertion wasGeneratedBy ECO_0000203 NP925520.RALqNuHjWV9lozrxRV_aNrHSrtSrmPGXVJLMTKic2cV7c130_provenance.