Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP936560.RA9CV_9N0mwjVhHOUGAe4K9Wl5J64AIt6oewRTt1cwzfs130_assertion> ?p ?o ?g. }
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- NP936560.RA9CV_9N0mwjVhHOUGAe4K9Wl5J64AIt6oewRTt1cwzfs130_assertion type Assertion NP936560.RA9CV_9N0mwjVhHOUGAe4K9Wl5J64AIt6oewRTt1cwzfs130_head.
- NP936560.RA9CV_9N0mwjVhHOUGAe4K9Wl5J64AIt6oewRTt1cwzfs130_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." NP936560.RA9CV_9N0mwjVhHOUGAe4K9Wl5J64AIt6oewRTt1cwzfs130_provenance.
- NP936560.RA9CV_9N0mwjVhHOUGAe4K9Wl5J64AIt6oewRTt1cwzfs130_assertion evidence source_evidence_literature NP936560.RA9CV_9N0mwjVhHOUGAe4K9Wl5J64AIt6oewRTt1cwzfs130_provenance.
- NP936560.RA9CV_9N0mwjVhHOUGAe4K9Wl5J64AIt6oewRTt1cwzfs130_assertion SIO_000772 22057234 NP936560.RA9CV_9N0mwjVhHOUGAe4K9Wl5J64AIt6oewRTt1cwzfs130_provenance.
- NP936560.RA9CV_9N0mwjVhHOUGAe4K9Wl5J64AIt6oewRTt1cwzfs130_assertion wasDerivedFrom befree-2016 NP936560.RA9CV_9N0mwjVhHOUGAe4K9Wl5J64AIt6oewRTt1cwzfs130_provenance.
- NP936560.RA9CV_9N0mwjVhHOUGAe4K9Wl5J64AIt6oewRTt1cwzfs130_assertion wasGeneratedBy ECO_0000203 NP936560.RA9CV_9N0mwjVhHOUGAe4K9Wl5J64AIt6oewRTt1cwzfs130_provenance.