Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP796220.RA65V4yjpBLOE7JqeC-VslAub1grDxH9Fsu6r9EdNvV2k130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP796220.RA65V4yjpBLOE7JqeC-VslAub1grDxH9Fsu6r9EdNvV2k130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP796220.RA65V4yjpBLOE7JqeC-VslAub1grDxH9Fsu6r9EdNvV2k130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP796220.RA65V4yjpBLOE7JqeC-VslAub1grDxH9Fsu6r9EdNvV2k130_provenance.
- NP796220.RA65V4yjpBLOE7JqeC-VslAub1grDxH9Fsu6r9EdNvV2k130_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." NP796220.RA65V4yjpBLOE7JqeC-VslAub1grDxH9Fsu6r9EdNvV2k130_provenance.
- NP796220.RA65V4yjpBLOE7JqeC-VslAub1grDxH9Fsu6r9EdNvV2k130_assertion evidence source_evidence_literature NP796220.RA65V4yjpBLOE7JqeC-VslAub1grDxH9Fsu6r9EdNvV2k130_provenance.
- NP796220.RA65V4yjpBLOE7JqeC-VslAub1grDxH9Fsu6r9EdNvV2k130_assertion SIO_000772 9603416 NP796220.RA65V4yjpBLOE7JqeC-VslAub1grDxH9Fsu6r9EdNvV2k130_provenance.
- NP796220.RA65V4yjpBLOE7JqeC-VslAub1grDxH9Fsu6r9EdNvV2k130_assertion wasDerivedFrom befree-20140225 NP796220.RA65V4yjpBLOE7JqeC-VslAub1grDxH9Fsu6r9EdNvV2k130_provenance.
- NP796220.RA65V4yjpBLOE7JqeC-VslAub1grDxH9Fsu6r9EdNvV2k130_assertion wasGeneratedBy ECO_0000203 NP796220.RA65V4yjpBLOE7JqeC-VslAub1grDxH9Fsu6r9EdNvV2k130_provenance.
- befree-20140225 importedOn "2014-02-25" NP796220.RA65V4yjpBLOE7JqeC-VslAub1grDxH9Fsu6r9EdNvV2k130_provenance.