Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP397190.RAwhaLmryg3BKISyZrBkUPHFv2XA_s1YWWKLGBzX2Fd6c130_assertion> ?p ?o ?g. }
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- NP397190.RAwhaLmryg3BKISyZrBkUPHFv2XA_s1YWWKLGBzX2Fd6c130_assertion type Assertion NP397190.RAwhaLmryg3BKISyZrBkUPHFv2XA_s1YWWKLGBzX2Fd6c130_head.
- NP397190.RAwhaLmryg3BKISyZrBkUPHFv2XA_s1YWWKLGBzX2Fd6c130_assertion description "[Mutation/deletion involving FLT3 D835 are found in more than 20% of cases with MLL intragenic abnormalities compared with 10% of AML with MLL translocation and 5% of adult AML with normal MLL status.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP397190.RAwhaLmryg3BKISyZrBkUPHFv2XA_s1YWWKLGBzX2Fd6c130_provenance.
- NP397190.RAwhaLmryg3BKISyZrBkUPHFv2XA_s1YWWKLGBzX2Fd6c130_assertion evidence source_evidence_literature NP397190.RAwhaLmryg3BKISyZrBkUPHFv2XA_s1YWWKLGBzX2Fd6c130_provenance.
- NP397190.RAwhaLmryg3BKISyZrBkUPHFv2XA_s1YWWKLGBzX2Fd6c130_assertion SIO_000772 12791658 NP397190.RAwhaLmryg3BKISyZrBkUPHFv2XA_s1YWWKLGBzX2Fd6c130_provenance.
- NP397190.RAwhaLmryg3BKISyZrBkUPHFv2XA_s1YWWKLGBzX2Fd6c130_assertion wasDerivedFrom befree-2016 NP397190.RAwhaLmryg3BKISyZrBkUPHFv2XA_s1YWWKLGBzX2Fd6c130_provenance.
- NP397190.RAwhaLmryg3BKISyZrBkUPHFv2XA_s1YWWKLGBzX2Fd6c130_assertion wasGeneratedBy ECO_0000203 NP397190.RAwhaLmryg3BKISyZrBkUPHFv2XA_s1YWWKLGBzX2Fd6c130_provenance.