Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP914483.RABqu8Q570UIuL0BfmgZto-hGF4A-PXKefx59n42bqYic130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP914483.RABqu8Q570UIuL0BfmgZto-hGF4A-PXKefx59n42bqYic130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP914483.RABqu8Q570UIuL0BfmgZto-hGF4A-PXKefx59n42bqYic130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP914483.RABqu8Q570UIuL0BfmgZto-hGF4A-PXKefx59n42bqYic130_provenance.
- NP914483.RABqu8Q570UIuL0BfmgZto-hGF4A-PXKefx59n42bqYic130_assertion description "[NUP98/NSD1 characterizes a novel poor prognostic group in acute myeloid leukemia with a distinct HOX gene expression pattern.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP914483.RABqu8Q570UIuL0BfmgZto-hGF4A-PXKefx59n42bqYic130_provenance.
- NP914483.RABqu8Q570UIuL0BfmgZto-hGF4A-PXKefx59n42bqYic130_assertion evidence source_evidence_literature NP914483.RABqu8Q570UIuL0BfmgZto-hGF4A-PXKefx59n42bqYic130_provenance.
- NP914483.RABqu8Q570UIuL0BfmgZto-hGF4A-PXKefx59n42bqYic130_assertion SIO_000772 21813447 NP914483.RABqu8Q570UIuL0BfmgZto-hGF4A-PXKefx59n42bqYic130_provenance.
- NP914483.RABqu8Q570UIuL0BfmgZto-hGF4A-PXKefx59n42bqYic130_assertion wasDerivedFrom befree-2016 NP914483.RABqu8Q570UIuL0BfmgZto-hGF4A-PXKefx59n42bqYic130_provenance.
- NP914483.RABqu8Q570UIuL0BfmgZto-hGF4A-PXKefx59n42bqYic130_assertion wasGeneratedBy ECO_0000203 NP914483.RABqu8Q570UIuL0BfmgZto-hGF4A-PXKefx59n42bqYic130_provenance.
- befree-2016 importedOn "2016-02-19" NP914483.RABqu8Q570UIuL0BfmgZto-hGF4A-PXKefx59n42bqYic130_provenance.