Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP501401.RAhgnaS1mBVZcugL78mQcBUHV7pxcFZvZBmY18zvxsaKw130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP501401.RAhgnaS1mBVZcugL78mQcBUHV7pxcFZvZBmY18zvxsaKw130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP501401.RAhgnaS1mBVZcugL78mQcBUHV7pxcFZvZBmY18zvxsaKw130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP501401.RAhgnaS1mBVZcugL78mQcBUHV7pxcFZvZBmY18zvxsaKw130_provenance.
- NP501401.RAhgnaS1mBVZcugL78mQcBUHV7pxcFZvZBmY18zvxsaKw130_assertion description "[The question arises whether this mutation is observed in those patients with ET and IMF who have also displayed previously described molecular markers, notably the ability to form endogenous erythroid colonies (EECs), overexpression of polycythemia rubra vera 1 (PRV-1), and decreased c-Mpl expression.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP501401.RAhgnaS1mBVZcugL78mQcBUHV7pxcFZvZBmY18zvxsaKw130_provenance.
- NP501401.RAhgnaS1mBVZcugL78mQcBUHV7pxcFZvZBmY18zvxsaKw130_assertion evidence source_evidence_literature NP501401.RAhgnaS1mBVZcugL78mQcBUHV7pxcFZvZBmY18zvxsaKw130_provenance.
- NP501401.RAhgnaS1mBVZcugL78mQcBUHV7pxcFZvZBmY18zvxsaKw130_assertion SIO_000772 15985544 NP501401.RAhgnaS1mBVZcugL78mQcBUHV7pxcFZvZBmY18zvxsaKw130_provenance.
- NP501401.RAhgnaS1mBVZcugL78mQcBUHV7pxcFZvZBmY18zvxsaKw130_assertion wasDerivedFrom befree-2016 NP501401.RAhgnaS1mBVZcugL78mQcBUHV7pxcFZvZBmY18zvxsaKw130_provenance.
- NP501401.RAhgnaS1mBVZcugL78mQcBUHV7pxcFZvZBmY18zvxsaKw130_assertion wasGeneratedBy ECO_0000203 NP501401.RAhgnaS1mBVZcugL78mQcBUHV7pxcFZvZBmY18zvxsaKw130_provenance.
- befree-2016 importedOn "2016-02-19" NP501401.RAhgnaS1mBVZcugL78mQcBUHV7pxcFZvZBmY18zvxsaKw130_provenance.