Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP474845.RABBk_P7FA_Vvebrdp4fOWRjgSLIfmQmY8jhlOz8aVQ9c130_assertion> ?p ?o ?g. }
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- NP474845.RABBk_P7FA_Vvebrdp4fOWRjgSLIfmQmY8jhlOz8aVQ9c130_assertion type Assertion NP474845.RABBk_P7FA_Vvebrdp4fOWRjgSLIfmQmY8jhlOz8aVQ9c130_head.
- NP474845.RABBk_P7FA_Vvebrdp4fOWRjgSLIfmQmY8jhlOz8aVQ9c130_assertion wasGeneratedBy ECO_0000203 NP474845.RABBk_P7FA_Vvebrdp4fOWRjgSLIfmQmY8jhlOz8aVQ9c130_provenance.
- NP474845.RABBk_P7FA_Vvebrdp4fOWRjgSLIfmQmY8jhlOz8aVQ9c130_assertion wasDerivedFrom befree-20150227 NP474845.RABBk_P7FA_Vvebrdp4fOWRjgSLIfmQmY8jhlOz8aVQ9c130_provenance.
- NP474845.RABBk_P7FA_Vvebrdp4fOWRjgSLIfmQmY8jhlOz8aVQ9c130_assertion SIO_000772 22809434 NP474845.RABBk_P7FA_Vvebrdp4fOWRjgSLIfmQmY8jhlOz8aVQ9c130_provenance.
- NP474845.RABBk_P7FA_Vvebrdp4fOWRjgSLIfmQmY8jhlOz8aVQ9c130_assertion evidence source_evidence_literature NP474845.RABBk_P7FA_Vvebrdp4fOWRjgSLIfmQmY8jhlOz8aVQ9c130_provenance.
- NP474845.RABBk_P7FA_Vvebrdp4fOWRjgSLIfmQmY8jhlOz8aVQ9c130_assertion description "[The results suggested that the IDH1 R132 mutation might be a recurrent gene alteration in ALL; patients carrying the mutation have a trend to aberrantly express myeloid antigen and the mutation may imply a dismal outcome.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP474845.RABBk_P7FA_Vvebrdp4fOWRjgSLIfmQmY8jhlOz8aVQ9c130_provenance.