Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP487117.RAh3tKa-Qdu6QDTpEhv2a9yxorLuA6O6YyT8EdlkUFmLc130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP487117.RAh3tKa-Qdu6QDTpEhv2a9yxorLuA6O6YyT8EdlkUFmLc130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP487117.RAh3tKa-Qdu6QDTpEhv2a9yxorLuA6O6YyT8EdlkUFmLc130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP487117.RAh3tKa-Qdu6QDTpEhv2a9yxorLuA6O6YyT8EdlkUFmLc130_provenance.
- NP487117.RAh3tKa-Qdu6QDTpEhv2a9yxorLuA6O6YyT8EdlkUFmLc130_assertion description "[Although all patients displayed a BII/common phenotype, supernumerary Ph and trisomy 8 were associated with higher expression of CD19 and CD22 and of CD19, CD34, CD45, and HLA-DR, respectively; in turn, cases with monosomy 7 showed lower CD19, CD22, CD34, and cCD79a and del(9p21)(+) blasts were CD13(-) and CD33(-).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP487117.RAh3tKa-Qdu6QDTpEhv2a9yxorLuA6O6YyT8EdlkUFmLc130_provenance.
- NP487117.RAh3tKa-Qdu6QDTpEhv2a9yxorLuA6O6YyT8EdlkUFmLc130_assertion evidence source_evidence_literature NP487117.RAh3tKa-Qdu6QDTpEhv2a9yxorLuA6O6YyT8EdlkUFmLc130_provenance.
- NP487117.RAh3tKa-Qdu6QDTpEhv2a9yxorLuA6O6YyT8EdlkUFmLc130_assertion SIO_000772 15789066 NP487117.RAh3tKa-Qdu6QDTpEhv2a9yxorLuA6O6YyT8EdlkUFmLc130_provenance.
- NP487117.RAh3tKa-Qdu6QDTpEhv2a9yxorLuA6O6YyT8EdlkUFmLc130_assertion wasDerivedFrom befree-2016 NP487117.RAh3tKa-Qdu6QDTpEhv2a9yxorLuA6O6YyT8EdlkUFmLc130_provenance.
- NP487117.RAh3tKa-Qdu6QDTpEhv2a9yxorLuA6O6YyT8EdlkUFmLc130_assertion wasGeneratedBy ECO_0000203 NP487117.RAh3tKa-Qdu6QDTpEhv2a9yxorLuA6O6YyT8EdlkUFmLc130_provenance.
- befree-2016 importedOn "2016-02-19" NP487117.RAh3tKa-Qdu6QDTpEhv2a9yxorLuA6O6YyT8EdlkUFmLc130_provenance.