Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP781423.RARY_eNpfNaUgZlNz9Vd-BW-kP0zq_v6l4hp2P9J-7RpY130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP781423.RARY_eNpfNaUgZlNz9Vd-BW-kP0zq_v6l4hp2P9J-7RpY130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP781423.RARY_eNpfNaUgZlNz9Vd-BW-kP0zq_v6l4hp2P9J-7RpY130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP781423.RARY_eNpfNaUgZlNz9Vd-BW-kP0zq_v6l4hp2P9J-7RpY130_provenance.
- NP781423.RARY_eNpfNaUgZlNz9Vd-BW-kP0zq_v6l4hp2P9J-7RpY130_assertion description "[We report two cases of AML who presented with well-characterised cytogenetic abnormalities at presentation: t(8;21) and t(15;17) respectively, and who, after achieving complete morphological and cytogenetic remissions post-autograft, developed MDS/AML associated with monosomy 7.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP781423.RARY_eNpfNaUgZlNz9Vd-BW-kP0zq_v6l4hp2P9J-7RpY130_provenance.
- NP781423.RARY_eNpfNaUgZlNz9Vd-BW-kP0zq_v6l4hp2P9J-7RpY130_assertion evidence source_evidence_literature NP781423.RARY_eNpfNaUgZlNz9Vd-BW-kP0zq_v6l4hp2P9J-7RpY130_provenance.
- NP781423.RARY_eNpfNaUgZlNz9Vd-BW-kP0zq_v6l4hp2P9J-7RpY130_assertion SIO_000772 9603416 NP781423.RARY_eNpfNaUgZlNz9Vd-BW-kP0zq_v6l4hp2P9J-7RpY130_provenance.
- NP781423.RARY_eNpfNaUgZlNz9Vd-BW-kP0zq_v6l4hp2P9J-7RpY130_assertion wasDerivedFrom befree-20150227 NP781423.RARY_eNpfNaUgZlNz9Vd-BW-kP0zq_v6l4hp2P9J-7RpY130_provenance.
- NP781423.RARY_eNpfNaUgZlNz9Vd-BW-kP0zq_v6l4hp2P9J-7RpY130_assertion wasGeneratedBy ECO_0000203 NP781423.RARY_eNpfNaUgZlNz9Vd-BW-kP0zq_v6l4hp2P9J-7RpY130_provenance.
- befree-20150227 importedOn "2015-02-27" NP781423.RARY_eNpfNaUgZlNz9Vd-BW-kP0zq_v6l4hp2P9J-7RpY130_provenance.