Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP251365.RAtbu2Q2SBndUR7EGaRV3nzIeC8yQ0RcQioLUixtNWY2Q130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP251365.RAtbu2Q2SBndUR7EGaRV3nzIeC8yQ0RcQioLUixtNWY2Q130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP251365.RAtbu2Q2SBndUR7EGaRV3nzIeC8yQ0RcQioLUixtNWY2Q130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP251365.RAtbu2Q2SBndUR7EGaRV3nzIeC8yQ0RcQioLUixtNWY2Q130_provenance.
- NP251365.RAtbu2Q2SBndUR7EGaRV3nzIeC8yQ0RcQioLUixtNWY2Q130_assertion description "[The inv(11)(p15q22) chromosome translocation of therapy-related myelodysplasia with NUP98-DDX10 and DDX10-NUP98 fusion transcripts.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP251365.RAtbu2Q2SBndUR7EGaRV3nzIeC8yQ0RcQioLUixtNWY2Q130_provenance.
- NP251365.RAtbu2Q2SBndUR7EGaRV3nzIeC8yQ0RcQioLUixtNWY2Q130_assertion evidence source_evidence_literature NP251365.RAtbu2Q2SBndUR7EGaRV3nzIeC8yQ0RcQioLUixtNWY2Q130_provenance.
- NP251365.RAtbu2Q2SBndUR7EGaRV3nzIeC8yQ0RcQioLUixtNWY2Q130_assertion SIO_000772 10222653 NP251365.RAtbu2Q2SBndUR7EGaRV3nzIeC8yQ0RcQioLUixtNWY2Q130_provenance.
- NP251365.RAtbu2Q2SBndUR7EGaRV3nzIeC8yQ0RcQioLUixtNWY2Q130_assertion wasDerivedFrom befree-2016 NP251365.RAtbu2Q2SBndUR7EGaRV3nzIeC8yQ0RcQioLUixtNWY2Q130_provenance.
- NP251365.RAtbu2Q2SBndUR7EGaRV3nzIeC8yQ0RcQioLUixtNWY2Q130_assertion wasGeneratedBy ECO_0000203 NP251365.RAtbu2Q2SBndUR7EGaRV3nzIeC8yQ0RcQioLUixtNWY2Q130_provenance.
- befree-2016 importedOn "2016-02-19" NP251365.RAtbu2Q2SBndUR7EGaRV3nzIeC8yQ0RcQioLUixtNWY2Q130_provenance.