Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP634521.RA5AdciavjHFC6vjriLkh82DMRLMgbLcy7BFbHF-LLWXo130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP634521.RA5AdciavjHFC6vjriLkh82DMRLMgbLcy7BFbHF-LLWXo130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP634521.RA5AdciavjHFC6vjriLkh82DMRLMgbLcy7BFbHF-LLWXo130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP634521.RA5AdciavjHFC6vjriLkh82DMRLMgbLcy7BFbHF-LLWXo130_provenance.
- NP634521.RA5AdciavjHFC6vjriLkh82DMRLMgbLcy7BFbHF-LLWXo130_assertion description "[Surprisingly, when we examined the bone marrow and peripheral mononuclear cells from patients with myelodysplastic syndrome (MDS) or leukemia secondary to MDS, we could still detect the exon-skipped form but little or none of the intact IRF-1 mRNA.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP634521.RA5AdciavjHFC6vjriLkh82DMRLMgbLcy7BFbHF-LLWXo130_provenance.
- NP634521.RA5AdciavjHFC6vjriLkh82DMRLMgbLcy7BFbHF-LLWXo130_assertion evidence source_evidence_literature NP634521.RA5AdciavjHFC6vjriLkh82DMRLMgbLcy7BFbHF-LLWXo130_provenance.
- NP634521.RA5AdciavjHFC6vjriLkh82DMRLMgbLcy7BFbHF-LLWXo130_assertion SIO_000772 7936656 NP634521.RA5AdciavjHFC6vjriLkh82DMRLMgbLcy7BFbHF-LLWXo130_provenance.
- NP634521.RA5AdciavjHFC6vjriLkh82DMRLMgbLcy7BFbHF-LLWXo130_assertion wasDerivedFrom befree-20140225 NP634521.RA5AdciavjHFC6vjriLkh82DMRLMgbLcy7BFbHF-LLWXo130_provenance.
- NP634521.RA5AdciavjHFC6vjriLkh82DMRLMgbLcy7BFbHF-LLWXo130_assertion wasGeneratedBy ECO_0000203 NP634521.RA5AdciavjHFC6vjriLkh82DMRLMgbLcy7BFbHF-LLWXo130_provenance.
- befree-20140225 importedOn "2014-02-25" NP634521.RA5AdciavjHFC6vjriLkh82DMRLMgbLcy7BFbHF-LLWXo130_provenance.