Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP90059.RAADrTFLSultwom4kRjECRUG_-r_2PyTTHsYKt2SZTF20130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP90059.RAADrTFLSultwom4kRjECRUG_-r_2PyTTHsYKt2SZTF20130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP90059.RAADrTFLSultwom4kRjECRUG_-r_2PyTTHsYKt2SZTF20130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP90059.RAADrTFLSultwom4kRjECRUG_-r_2PyTTHsYKt2SZTF20130_provenance.
- NP90059.RAADrTFLSultwom4kRjECRUG_-r_2PyTTHsYKt2SZTF20130_assertion description "[We examined 193 patients with myelodysplastic syndromes and 53 patients with acute myeloid leukemia arising from myelodysplastic syndromes for mutations in IDH1 (R132), IDH2 (R172 and R140), and NPM1 by direct sequencing.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP90059.RAADrTFLSultwom4kRjECRUG_-r_2PyTTHsYKt2SZTF20130_provenance.
- NP90059.RAADrTFLSultwom4kRjECRUG_-r_2PyTTHsYKt2SZTF20130_assertion evidence source_evidence_literature NP90059.RAADrTFLSultwom4kRjECRUG_-r_2PyTTHsYKt2SZTF20130_provenance.
- NP90059.RAADrTFLSultwom4kRjECRUG_-r_2PyTTHsYKt2SZTF20130_assertion SIO_000772 20494930 NP90059.RAADrTFLSultwom4kRjECRUG_-r_2PyTTHsYKt2SZTF20130_provenance.
- NP90059.RAADrTFLSultwom4kRjECRUG_-r_2PyTTHsYKt2SZTF20130_assertion wasDerivedFrom gad-20150221 NP90059.RAADrTFLSultwom4kRjECRUG_-r_2PyTTHsYKt2SZTF20130_provenance.
- NP90059.RAADrTFLSultwom4kRjECRUG_-r_2PyTTHsYKt2SZTF20130_assertion wasGeneratedBy ECO_0000203 NP90059.RAADrTFLSultwom4kRjECRUG_-r_2PyTTHsYKt2SZTF20130_provenance.
- gad-20150221 importedOn "2015-02-21" NP90059.RAADrTFLSultwom4kRjECRUG_-r_2PyTTHsYKt2SZTF20130_provenance.