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- source_evidence_literature type ECO_0000212 NP755559.RAMmphunLBf-njhQ6t82HtCGan2mrDfx4AzeXZHNZDpEA130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP755559.RAMmphunLBf-njhQ6t82HtCGan2mrDfx4AzeXZHNZDpEA130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP755559.RAMmphunLBf-njhQ6t82HtCGan2mrDfx4AzeXZHNZDpEA130_provenance.
- NP755559.RAMmphunLBf-njhQ6t82HtCGan2mrDfx4AzeXZHNZDpEA130_assertion wasGeneratedBy ECO_0000203 NP755559.RAMmphunLBf-njhQ6t82HtCGan2mrDfx4AzeXZHNZDpEA130_provenance.
- NP755559.RAMmphunLBf-njhQ6t82HtCGan2mrDfx4AzeXZHNZDpEA130_assertion wasDerivedFrom befree-20140225 NP755559.RAMmphunLBf-njhQ6t82HtCGan2mrDfx4AzeXZHNZDpEA130_provenance.
- NP755559.RAMmphunLBf-njhQ6t82HtCGan2mrDfx4AzeXZHNZDpEA130_assertion SIO_000772 14506644 NP755559.RAMmphunLBf-njhQ6t82HtCGan2mrDfx4AzeXZHNZDpEA130_provenance.
- NP755559.RAMmphunLBf-njhQ6t82HtCGan2mrDfx4AzeXZHNZDpEA130_assertion evidence source_evidence_literature NP755559.RAMmphunLBf-njhQ6t82HtCGan2mrDfx4AzeXZHNZDpEA130_provenance.
- NP755559.RAMmphunLBf-njhQ6t82HtCGan2mrDfx4AzeXZHNZDpEA130_assertion description "[These findings suggest that an NPM/MLF1 fusion is the primary molecular abnormality in t(3;5) MDS and AML with multilineage dysplasia, and also that cases with NPM/MLF1 may be clinically distinct from other MDS-associated disease.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP755559.RAMmphunLBf-njhQ6t82HtCGan2mrDfx4AzeXZHNZDpEA130_provenance.
- befree-20140225 importedOn "2014-02-25" NP755559.RAMmphunLBf-njhQ6t82HtCGan2mrDfx4AzeXZHNZDpEA130_provenance.