Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP442632.RA90S7pOtx-Bg1qN76tGqg6jdyzHv_89Ho_vloJjwYhzo130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP442632.RA90S7pOtx-Bg1qN76tGqg6jdyzHv_89Ho_vloJjwYhzo130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP442632.RA90S7pOtx-Bg1qN76tGqg6jdyzHv_89Ho_vloJjwYhzo130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP442632.RA90S7pOtx-Bg1qN76tGqg6jdyzHv_89Ho_vloJjwYhzo130_provenance.
- NP442632.RA90S7pOtx-Bg1qN76tGqg6jdyzHv_89Ho_vloJjwYhzo130_assertion description "[Even more, molecular markers such as MLL partial tandem duplications (MLL-PTD) or FLT3 length mutations (FLT3-LM) were found to characterize specific subtypes of AML and completed the genetic marker profile.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP442632.RA90S7pOtx-Bg1qN76tGqg6jdyzHv_89Ho_vloJjwYhzo130_provenance.
- NP442632.RA90S7pOtx-Bg1qN76tGqg6jdyzHv_89Ho_vloJjwYhzo130_assertion evidence source_evidence_literature NP442632.RA90S7pOtx-Bg1qN76tGqg6jdyzHv_89Ho_vloJjwYhzo130_provenance.
- NP442632.RA90S7pOtx-Bg1qN76tGqg6jdyzHv_89Ho_vloJjwYhzo130_assertion SIO_000772 15124693 NP442632.RA90S7pOtx-Bg1qN76tGqg6jdyzHv_89Ho_vloJjwYhzo130_provenance.
- NP442632.RA90S7pOtx-Bg1qN76tGqg6jdyzHv_89Ho_vloJjwYhzo130_assertion wasDerivedFrom befree-2016 NP442632.RA90S7pOtx-Bg1qN76tGqg6jdyzHv_89Ho_vloJjwYhzo130_provenance.
- NP442632.RA90S7pOtx-Bg1qN76tGqg6jdyzHv_89Ho_vloJjwYhzo130_assertion wasGeneratedBy ECO_0000203 NP442632.RA90S7pOtx-Bg1qN76tGqg6jdyzHv_89Ho_vloJjwYhzo130_provenance.
- befree-2016 importedOn "2016-02-19" NP442632.RA90S7pOtx-Bg1qN76tGqg6jdyzHv_89Ho_vloJjwYhzo130_provenance.