Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP760253.RAMOE1O78D7pnNKD4YMWkZjgBCPz3BOPAOxA9bBhwOTlQ130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP760253.RAMOE1O78D7pnNKD4YMWkZjgBCPz3BOPAOxA9bBhwOTlQ130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP760253.RAMOE1O78D7pnNKD4YMWkZjgBCPz3BOPAOxA9bBhwOTlQ130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP760253.RAMOE1O78D7pnNKD4YMWkZjgBCPz3BOPAOxA9bBhwOTlQ130_provenance.
- befree-2016 importedOn "2016-02-19" NP760253.RAMOE1O78D7pnNKD4YMWkZjgBCPz3BOPAOxA9bBhwOTlQ130_provenance.
- NP760253.RAMOE1O78D7pnNKD4YMWkZjgBCPz3BOPAOxA9bBhwOTlQ130_assertion wasGeneratedBy ECO_0000203 NP760253.RAMOE1O78D7pnNKD4YMWkZjgBCPz3BOPAOxA9bBhwOTlQ130_provenance.
- NP760253.RAMOE1O78D7pnNKD4YMWkZjgBCPz3BOPAOxA9bBhwOTlQ130_assertion wasDerivedFrom befree-2016 NP760253.RAMOE1O78D7pnNKD4YMWkZjgBCPz3BOPAOxA9bBhwOTlQ130_provenance.
- NP760253.RAMOE1O78D7pnNKD4YMWkZjgBCPz3BOPAOxA9bBhwOTlQ130_assertion SIO_000772 19717645 NP760253.RAMOE1O78D7pnNKD4YMWkZjgBCPz3BOPAOxA9bBhwOTlQ130_provenance.
- NP760253.RAMOE1O78D7pnNKD4YMWkZjgBCPz3BOPAOxA9bBhwOTlQ130_assertion evidence source_evidence_literature NP760253.RAMOE1O78D7pnNKD4YMWkZjgBCPz3BOPAOxA9bBhwOTlQ130_provenance.
- NP760253.RAMOE1O78D7pnNKD4YMWkZjgBCPz3BOPAOxA9bBhwOTlQ130_assertion description "[In this study we also found that IGHV unmutated, high expression of ZAP-70 protein, and low expression of the miR-223, miR-29c, miR-29b, and miR-181 family were strongly associated with disease progression in CLL cases harboring 17p deletion, whereas in those harboring trisomy 12 only high expression of the miR-181a, among the analyzed parameters, suggested more aggressive disease.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP760253.RAMOE1O78D7pnNKD4YMWkZjgBCPz3BOPAOxA9bBhwOTlQ130_provenance.