Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP1293765.RAC3t0os7kkwMRT1G2gGTUD6rJ99nXJKJKtve8ugTSIoI130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP1293765.RAC3t0os7kkwMRT1G2gGTUD6rJ99nXJKJKtve8ugTSIoI130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP1293765.RAC3t0os7kkwMRT1G2gGTUD6rJ99nXJKJKtve8ugTSIoI130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP1293765.RAC3t0os7kkwMRT1G2gGTUD6rJ99nXJKJKtve8ugTSIoI130_provenance.
- NP1293765.RAC3t0os7kkwMRT1G2gGTUD6rJ99nXJKJKtve8ugTSIoI130_assertion description "[Although loss or near-complete loss of the hematopoietic transcription factor PU.1 induces acute myeloid leukemia (AML) in mice, a similar degree of PU.1 impairment is exceedingly rare in human AML; yet, moderate PU.1 inhibition is common in AML patients.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1293765.RAC3t0os7kkwMRT1G2gGTUD6rJ99nXJKJKtve8ugTSIoI130_provenance.
- NP1293765.RAC3t0os7kkwMRT1G2gGTUD6rJ99nXJKJKtve8ugTSIoI130_assertion evidence source_evidence_literature NP1293765.RAC3t0os7kkwMRT1G2gGTUD6rJ99nXJKJKtve8ugTSIoI130_provenance.
- NP1293765.RAC3t0os7kkwMRT1G2gGTUD6rJ99nXJKJKtve8ugTSIoI130_assertion SIO_000772 26343801 NP1293765.RAC3t0os7kkwMRT1G2gGTUD6rJ99nXJKJKtve8ugTSIoI130_provenance.
- NP1293765.RAC3t0os7kkwMRT1G2gGTUD6rJ99nXJKJKtve8ugTSIoI130_assertion wasDerivedFrom befree-2016 NP1293765.RAC3t0os7kkwMRT1G2gGTUD6rJ99nXJKJKtve8ugTSIoI130_provenance.
- NP1293765.RAC3t0os7kkwMRT1G2gGTUD6rJ99nXJKJKtve8ugTSIoI130_assertion wasGeneratedBy ECO_0000203 NP1293765.RAC3t0os7kkwMRT1G2gGTUD6rJ99nXJKJKtve8ugTSIoI130_provenance.
- befree-2016 importedOn "2016-02-19" NP1293765.RAC3t0os7kkwMRT1G2gGTUD6rJ99nXJKJKtve8ugTSIoI130_provenance.