Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP474823.RAUi9He76Y0LtOXTYUb5JrlnRl0QU9AxE8qvC2q3T24AU130_assertion> ?p ?o ?g. }
Showing items 1 to 6 of
6
with 100 items per page.
- NP474823.RAUi9He76Y0LtOXTYUb5JrlnRl0QU9AxE8qvC2q3T24AU130_assertion type Assertion NP474823.RAUi9He76Y0LtOXTYUb5JrlnRl0QU9AxE8qvC2q3T24AU130_head.
- NP474823.RAUi9He76Y0LtOXTYUb5JrlnRl0QU9AxE8qvC2q3T24AU130_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." NP474823.RAUi9He76Y0LtOXTYUb5JrlnRl0QU9AxE8qvC2q3T24AU130_provenance.
- NP474823.RAUi9He76Y0LtOXTYUb5JrlnRl0QU9AxE8qvC2q3T24AU130_assertion evidence source_evidence_literature NP474823.RAUi9He76Y0LtOXTYUb5JrlnRl0QU9AxE8qvC2q3T24AU130_provenance.
- NP474823.RAUi9He76Y0LtOXTYUb5JrlnRl0QU9AxE8qvC2q3T24AU130_assertion SIO_000772 22057234 NP474823.RAUi9He76Y0LtOXTYUb5JrlnRl0QU9AxE8qvC2q3T24AU130_provenance.
- NP474823.RAUi9He76Y0LtOXTYUb5JrlnRl0QU9AxE8qvC2q3T24AU130_assertion wasDerivedFrom befree-20150227 NP474823.RAUi9He76Y0LtOXTYUb5JrlnRl0QU9AxE8qvC2q3T24AU130_provenance.
- NP474823.RAUi9He76Y0LtOXTYUb5JrlnRl0QU9AxE8qvC2q3T24AU130_assertion wasGeneratedBy ECO_0000203 NP474823.RAUi9He76Y0LtOXTYUb5JrlnRl0QU9AxE8qvC2q3T24AU130_provenance.