Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP936556.RACTFLQzhX-OOpEq2D8xfhYKO5W9empp_sAc2IL3mBKog130_assertion> ?p ?o ?g. }
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- NP936556.RACTFLQzhX-OOpEq2D8xfhYKO5W9empp_sAc2IL3mBKog130_assertion type Assertion NP936556.RACTFLQzhX-OOpEq2D8xfhYKO5W9empp_sAc2IL3mBKog130_head.
- NP936556.RACTFLQzhX-OOpEq2D8xfhYKO5W9empp_sAc2IL3mBKog130_assertion description "[We report somatic heterozygous mutations in IDH1 (c.394C>T encoding an R132C substitution and c.395G>A encoding an R132H substitution) or IDH2 (c.516G>C encoding R172S) in 87% of enchondromas (benign cartilage tumors) and in 70% of spindle cell hemangiomas (benign vascular lesions).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP936556.RACTFLQzhX-OOpEq2D8xfhYKO5W9empp_sAc2IL3mBKog130_provenance.
- NP936556.RACTFLQzhX-OOpEq2D8xfhYKO5W9empp_sAc2IL3mBKog130_assertion evidence source_evidence_literature NP936556.RACTFLQzhX-OOpEq2D8xfhYKO5W9empp_sAc2IL3mBKog130_provenance.
- NP936556.RACTFLQzhX-OOpEq2D8xfhYKO5W9empp_sAc2IL3mBKog130_assertion SIO_000772 22057234 NP936556.RACTFLQzhX-OOpEq2D8xfhYKO5W9empp_sAc2IL3mBKog130_provenance.
- NP936556.RACTFLQzhX-OOpEq2D8xfhYKO5W9empp_sAc2IL3mBKog130_assertion wasDerivedFrom befree-2016 NP936556.RACTFLQzhX-OOpEq2D8xfhYKO5W9empp_sAc2IL3mBKog130_provenance.
- NP936556.RACTFLQzhX-OOpEq2D8xfhYKO5W9empp_sAc2IL3mBKog130_assertion wasGeneratedBy ECO_0000203 NP936556.RACTFLQzhX-OOpEq2D8xfhYKO5W9empp_sAc2IL3mBKog130_provenance.