Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP750519.RALJr7kBbXTtw_WKeOcPxouq7Z2U-e5RhSDoyri8YLhhI130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP750519.RALJr7kBbXTtw_WKeOcPxouq7Z2U-e5RhSDoyri8YLhhI130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP750519.RALJr7kBbXTtw_WKeOcPxouq7Z2U-e5RhSDoyri8YLhhI130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP750519.RALJr7kBbXTtw_WKeOcPxouq7Z2U-e5RhSDoyri8YLhhI130_provenance.
- befree-20150227 importedOn "2015-02-27" NP750519.RALJr7kBbXTtw_WKeOcPxouq7Z2U-e5RhSDoyri8YLhhI130_provenance.
- NP750519.RALJr7kBbXTtw_WKeOcPxouq7Z2U-e5RhSDoyri8YLhhI130_assertion wasGeneratedBy ECO_0000203 NP750519.RALJr7kBbXTtw_WKeOcPxouq7Z2U-e5RhSDoyri8YLhhI130_provenance.
- NP750519.RALJr7kBbXTtw_WKeOcPxouq7Z2U-e5RhSDoyri8YLhhI130_assertion wasDerivedFrom befree-20150227 NP750519.RALJr7kBbXTtw_WKeOcPxouq7Z2U-e5RhSDoyri8YLhhI130_provenance.
- NP750519.RALJr7kBbXTtw_WKeOcPxouq7Z2U-e5RhSDoyri8YLhhI130_assertion SIO_000772 8037181 NP750519.RALJr7kBbXTtw_WKeOcPxouq7Z2U-e5RhSDoyri8YLhhI130_provenance.
- NP750519.RALJr7kBbXTtw_WKeOcPxouq7Z2U-e5RhSDoyri8YLhhI130_assertion evidence source_evidence_literature NP750519.RALJr7kBbXTtw_WKeOcPxouq7Z2U-e5RhSDoyri8YLhhI130_provenance.
- NP750519.RALJr7kBbXTtw_WKeOcPxouq7Z2U-e5RhSDoyri8YLhhI130_assertion description "[We have previously reported the absence of mutations within exons 5-9 of the p53 gene in a panel of 30 cases of acute promyelocytic leukemia (APL), which represent the M3 FAB type of acute myeloid leukemia (AML).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP750519.RALJr7kBbXTtw_WKeOcPxouq7Z2U-e5RhSDoyri8YLhhI130_provenance.