Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP478377.RAV2hQv1Ot3Qo7yr5JKq0fNRs03kiBlm0bejmCw4eQzc8130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP478377.RAV2hQv1Ot3Qo7yr5JKq0fNRs03kiBlm0bejmCw4eQzc8130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP478377.RAV2hQv1Ot3Qo7yr5JKq0fNRs03kiBlm0bejmCw4eQzc8130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP478377.RAV2hQv1Ot3Qo7yr5JKq0fNRs03kiBlm0bejmCw4eQzc8130_provenance.
- NP478377.RAV2hQv1Ot3Qo7yr5JKq0fNRs03kiBlm0bejmCw4eQzc8130_assertion description "[NUP98/NSD1-positive AML cases had significantly higher white blood cell counts (median, 147 � 10?/L), more frequent FAB-M4/M5 morphology (in 63%), and more CN-AML (in 78%), FLT3/internal tandem duplication (in 91%) and WT1 mutations (in 45%) than NUP98/NSD1-negative cases.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP478377.RAV2hQv1Ot3Qo7yr5JKq0fNRs03kiBlm0bejmCw4eQzc8130_provenance.
- NP478377.RAV2hQv1Ot3Qo7yr5JKq0fNRs03kiBlm0bejmCw4eQzc8130_assertion evidence source_evidence_literature NP478377.RAV2hQv1Ot3Qo7yr5JKq0fNRs03kiBlm0bejmCw4eQzc8130_provenance.
- NP478377.RAV2hQv1Ot3Qo7yr5JKq0fNRs03kiBlm0bejmCw4eQzc8130_assertion SIO_000772 21813447 NP478377.RAV2hQv1Ot3Qo7yr5JKq0fNRs03kiBlm0bejmCw4eQzc8130_provenance.
- NP478377.RAV2hQv1Ot3Qo7yr5JKq0fNRs03kiBlm0bejmCw4eQzc8130_assertion wasDerivedFrom befree-20140225 NP478377.RAV2hQv1Ot3Qo7yr5JKq0fNRs03kiBlm0bejmCw4eQzc8130_provenance.
- NP478377.RAV2hQv1Ot3Qo7yr5JKq0fNRs03kiBlm0bejmCw4eQzc8130_assertion wasGeneratedBy ECO_0000203 NP478377.RAV2hQv1Ot3Qo7yr5JKq0fNRs03kiBlm0bejmCw4eQzc8130_provenance.
- befree-20140225 importedOn "2014-02-25" NP478377.RAV2hQv1Ot3Qo7yr5JKq0fNRs03kiBlm0bejmCw4eQzc8130_provenance.