Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP138759.RAnX--50OXOA_KNFwlPvCH_K8Dh8WRGnSYyPwqRGodK-E130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP138759.RAnX--50OXOA_KNFwlPvCH_K8Dh8WRGnSYyPwqRGodK-E130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP138759.RAnX--50OXOA_KNFwlPvCH_K8Dh8WRGnSYyPwqRGodK-E130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP138759.RAnX--50OXOA_KNFwlPvCH_K8Dh8WRGnSYyPwqRGodK-E130_provenance.
- NP138759.RAnX--50OXOA_KNFwlPvCH_K8Dh8WRGnSYyPwqRGodK-E130_assertion description "[Frequent genomic abnormalities in acute myeloid leukemia/myelodysplastic syndrome with normal karyotype.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP138759.RAnX--50OXOA_KNFwlPvCH_K8Dh8WRGnSYyPwqRGodK-E130_provenance.
- NP138759.RAnX--50OXOA_KNFwlPvCH_K8Dh8WRGnSYyPwqRGodK-E130_assertion evidence source_evidence_literature NP138759.RAnX--50OXOA_KNFwlPvCH_K8Dh8WRGnSYyPwqRGodK-E130_provenance.
- NP138759.RAnX--50OXOA_KNFwlPvCH_K8Dh8WRGnSYyPwqRGodK-E130_assertion SIO_000772 19144660 NP138759.RAnX--50OXOA_KNFwlPvCH_K8Dh8WRGnSYyPwqRGodK-E130_provenance.
- NP138759.RAnX--50OXOA_KNFwlPvCH_K8Dh8WRGnSYyPwqRGodK-E130_assertion wasDerivedFrom gad-20150221 NP138759.RAnX--50OXOA_KNFwlPvCH_K8Dh8WRGnSYyPwqRGodK-E130_provenance.
- NP138759.RAnX--50OXOA_KNFwlPvCH_K8Dh8WRGnSYyPwqRGodK-E130_assertion wasGeneratedBy ECO_0000203 NP138759.RAnX--50OXOA_KNFwlPvCH_K8Dh8WRGnSYyPwqRGodK-E130_provenance.
- gad-20150221 importedOn "2015-02-21" NP138759.RAnX--50OXOA_KNFwlPvCH_K8Dh8WRGnSYyPwqRGodK-E130_provenance.