Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP474845.RABBk_P7FA_Vvebrdp4fOWRjgSLIfmQmY8jhlOz8aVQ9c130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP474845.RABBk_P7FA_Vvebrdp4fOWRjgSLIfmQmY8jhlOz8aVQ9c130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP474845.RABBk_P7FA_Vvebrdp4fOWRjgSLIfmQmY8jhlOz8aVQ9c130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP474845.RABBk_P7FA_Vvebrdp4fOWRjgSLIfmQmY8jhlOz8aVQ9c130_provenance.
- befree-20150227 importedOn "2015-02-27" NP474845.RABBk_P7FA_Vvebrdp4fOWRjgSLIfmQmY8jhlOz8aVQ9c130_provenance.
- 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.