Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP788007.RABPiM5LSOelMJXhyeYBgxIcitjzgANXjC8tnhp5MqN_U130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP788007.RABPiM5LSOelMJXhyeYBgxIcitjzgANXjC8tnhp5MqN_U130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP788007.RABPiM5LSOelMJXhyeYBgxIcitjzgANXjC8tnhp5MqN_U130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP788007.RABPiM5LSOelMJXhyeYBgxIcitjzgANXjC8tnhp5MqN_U130_provenance.
- NP788007.RABPiM5LSOelMJXhyeYBgxIcitjzgANXjC8tnhp5MqN_U130_assertion description "[Here we show that reduced gene dosage of NR4A1 and NR4A3 in hypoallelic (NR4A1(+/-)NR4A3(-/-) or NR4A1(-/-)NR4A3(+/-)) mice below a critical threshold leads to a chronic myeloid malignancy that closely recapitulates the pathologic features of mixed myelodysplastic/myeloproliferative neoplasms (MDS/MPNs) with progression to AML in rare cases.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP788007.RABPiM5LSOelMJXhyeYBgxIcitjzgANXjC8tnhp5MqN_U130_provenance.
- NP788007.RABPiM5LSOelMJXhyeYBgxIcitjzgANXjC8tnhp5MqN_U130_assertion evidence source_evidence_literature NP788007.RABPiM5LSOelMJXhyeYBgxIcitjzgANXjC8tnhp5MqN_U130_provenance.
- NP788007.RABPiM5LSOelMJXhyeYBgxIcitjzgANXjC8tnhp5MqN_U130_assertion SIO_000772 21205929 NP788007.RABPiM5LSOelMJXhyeYBgxIcitjzgANXjC8tnhp5MqN_U130_provenance.
- NP788007.RABPiM5LSOelMJXhyeYBgxIcitjzgANXjC8tnhp5MqN_U130_assertion wasDerivedFrom befree-20150227 NP788007.RABPiM5LSOelMJXhyeYBgxIcitjzgANXjC8tnhp5MqN_U130_provenance.
- NP788007.RABPiM5LSOelMJXhyeYBgxIcitjzgANXjC8tnhp5MqN_U130_assertion wasGeneratedBy ECO_0000203 NP788007.RABPiM5LSOelMJXhyeYBgxIcitjzgANXjC8tnhp5MqN_U130_provenance.
- befree-20150227 importedOn "2015-02-27" NP788007.RABPiM5LSOelMJXhyeYBgxIcitjzgANXjC8tnhp5MqN_U130_provenance.