Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP402996.RAj4Ketz7LGBqPt94nWr3ZuJCNMMmikm_N1M9utbVQ810130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP402996.RAj4Ketz7LGBqPt94nWr3ZuJCNMMmikm_N1M9utbVQ810130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP402996.RAj4Ketz7LGBqPt94nWr3ZuJCNMMmikm_N1M9utbVQ810130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP402996.RAj4Ketz7LGBqPt94nWr3ZuJCNMMmikm_N1M9utbVQ810130_provenance.
- NP402996.RAj4Ketz7LGBqPt94nWr3ZuJCNMMmikm_N1M9utbVQ810130_assertion description "[One-year mortality was also high, especially for the MM-MDS subgroup with trisomy 8 within a MM signature karyotype (87%vs 34% in its absence, P < 0.001).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP402996.RAj4Ketz7LGBqPt94nWr3ZuJCNMMmikm_N1M9utbVQ810130_provenance.
- NP402996.RAj4Ketz7LGBqPt94nWr3ZuJCNMMmikm_N1M9utbVQ810130_assertion evidence source_evidence_literature NP402996.RAj4Ketz7LGBqPt94nWr3ZuJCNMMmikm_N1M9utbVQ810130_provenance.
- NP402996.RAj4Ketz7LGBqPt94nWr3ZuJCNMMmikm_N1M9utbVQ810130_assertion SIO_000772 12877670 NP402996.RAj4Ketz7LGBqPt94nWr3ZuJCNMMmikm_N1M9utbVQ810130_provenance.
- NP402996.RAj4Ketz7LGBqPt94nWr3ZuJCNMMmikm_N1M9utbVQ810130_assertion wasDerivedFrom befree-2016 NP402996.RAj4Ketz7LGBqPt94nWr3ZuJCNMMmikm_N1M9utbVQ810130_provenance.
- NP402996.RAj4Ketz7LGBqPt94nWr3ZuJCNMMmikm_N1M9utbVQ810130_assertion wasGeneratedBy ECO_0000203 NP402996.RAj4Ketz7LGBqPt94nWr3ZuJCNMMmikm_N1M9utbVQ810130_provenance.
- befree-2016 importedOn "2016-02-19" NP402996.RAj4Ketz7LGBqPt94nWr3ZuJCNMMmikm_N1M9utbVQ810130_provenance.