Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP469784.RAuuCNK6uRe9M4FHiKEPkYb7h_1dUKcLRYaMuDP3k0jJ4130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP469784.RAuuCNK6uRe9M4FHiKEPkYb7h_1dUKcLRYaMuDP3k0jJ4130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP469784.RAuuCNK6uRe9M4FHiKEPkYb7h_1dUKcLRYaMuDP3k0jJ4130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP469784.RAuuCNK6uRe9M4FHiKEPkYb7h_1dUKcLRYaMuDP3k0jJ4130_provenance.
- NP469784.RAuuCNK6uRe9M4FHiKEPkYb7h_1dUKcLRYaMuDP3k0jJ4130_assertion description "[Real-time quantification of FLT3 in 141 cases of AML showed that all cases with FLT3 D835 express high level transcripts, whereas FLT3-ITD AML can be divided into cases with high-level FLT3 expression, which belong essentially to the monocytic lineage, and those with relatively low-level expression, which predominantly demonstrate PML-RARA and DEK-CAN.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP469784.RAuuCNK6uRe9M4FHiKEPkYb7h_1dUKcLRYaMuDP3k0jJ4130_provenance.
- NP469784.RAuuCNK6uRe9M4FHiKEPkYb7h_1dUKcLRYaMuDP3k0jJ4130_assertion evidence source_evidence_literature NP469784.RAuuCNK6uRe9M4FHiKEPkYb7h_1dUKcLRYaMuDP3k0jJ4130_provenance.
- NP469784.RAuuCNK6uRe9M4FHiKEPkYb7h_1dUKcLRYaMuDP3k0jJ4130_assertion SIO_000772 12791658 NP469784.RAuuCNK6uRe9M4FHiKEPkYb7h_1dUKcLRYaMuDP3k0jJ4130_provenance.
- NP469784.RAuuCNK6uRe9M4FHiKEPkYb7h_1dUKcLRYaMuDP3k0jJ4130_assertion wasDerivedFrom befree-20140225 NP469784.RAuuCNK6uRe9M4FHiKEPkYb7h_1dUKcLRYaMuDP3k0jJ4130_provenance.
- NP469784.RAuuCNK6uRe9M4FHiKEPkYb7h_1dUKcLRYaMuDP3k0jJ4130_assertion wasGeneratedBy ECO_0000203 NP469784.RAuuCNK6uRe9M4FHiKEPkYb7h_1dUKcLRYaMuDP3k0jJ4130_provenance.
- befree-20140225 importedOn "2014-02-25" NP469784.RAuuCNK6uRe9M4FHiKEPkYb7h_1dUKcLRYaMuDP3k0jJ4130_provenance.