Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP925520.RALqNuHjWV9lozrxRV_aNrHSrtSrmPGXVJLMTKic2cV7c130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP925520.RALqNuHjWV9lozrxRV_aNrHSrtSrmPGXVJLMTKic2cV7c130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP925520.RALqNuHjWV9lozrxRV_aNrHSrtSrmPGXVJLMTKic2cV7c130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP925520.RALqNuHjWV9lozrxRV_aNrHSrtSrmPGXVJLMTKic2cV7c130_provenance.
- 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.
- befree-20140225 importedOn "2014-02-25" NP925520.RALqNuHjWV9lozrxRV_aNrHSrtSrmPGXVJLMTKic2cV7c130_provenance.