Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP979929.RAo4fDYu1OPXdT9s4fKPkSnSkxuRaT9p4mEOzmrD2pJ90130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP979929.RAo4fDYu1OPXdT9s4fKPkSnSkxuRaT9p4mEOzmrD2pJ90130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP979929.RAo4fDYu1OPXdT9s4fKPkSnSkxuRaT9p4mEOzmrD2pJ90130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP979929.RAo4fDYu1OPXdT9s4fKPkSnSkxuRaT9p4mEOzmrD2pJ90130_provenance.
- NP979929.RAo4fDYu1OPXdT9s4fKPkSnSkxuRaT9p4mEOzmrD2pJ90130_assertion description "[Chromosomal alterations and mutation of FLT3 (FMS-like tyrosine kinase 3) tyrosine kinase receptor are the frequent genetic alterations in acute myeloid leukemia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP979929.RAo4fDYu1OPXdT9s4fKPkSnSkxuRaT9p4mEOzmrD2pJ90130_provenance.
- NP979929.RAo4fDYu1OPXdT9s4fKPkSnSkxuRaT9p4mEOzmrD2pJ90130_assertion evidence source_evidence_literature NP979929.RAo4fDYu1OPXdT9s4fKPkSnSkxuRaT9p4mEOzmrD2pJ90130_provenance.
- NP979929.RAo4fDYu1OPXdT9s4fKPkSnSkxuRaT9p4mEOzmrD2pJ90130_assertion SIO_000772 22562027 NP979929.RAo4fDYu1OPXdT9s4fKPkSnSkxuRaT9p4mEOzmrD2pJ90130_provenance.
- NP979929.RAo4fDYu1OPXdT9s4fKPkSnSkxuRaT9p4mEOzmrD2pJ90130_assertion wasDerivedFrom befree-2016 NP979929.RAo4fDYu1OPXdT9s4fKPkSnSkxuRaT9p4mEOzmrD2pJ90130_provenance.
- NP979929.RAo4fDYu1OPXdT9s4fKPkSnSkxuRaT9p4mEOzmrD2pJ90130_assertion wasGeneratedBy ECO_0000203 NP979929.RAo4fDYu1OPXdT9s4fKPkSnSkxuRaT9p4mEOzmrD2pJ90130_provenance.
- befree-2016 importedOn "2016-02-19" NP979929.RAo4fDYu1OPXdT9s4fKPkSnSkxuRaT9p4mEOzmrD2pJ90130_provenance.