Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP913971.RArHG7anJvhmGuZd1Rzd8JGmEFTbvxMfP5OCzWrVgHhII130_assertion> ?p ?o ?g. }
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- NP913971.RArHG7anJvhmGuZd1Rzd8JGmEFTbvxMfP5OCzWrVgHhII130_assertion type Assertion NP913971.RArHG7anJvhmGuZd1Rzd8JGmEFTbvxMfP5OCzWrVgHhII130_head.
- NP913971.RArHG7anJvhmGuZd1Rzd8JGmEFTbvxMfP5OCzWrVgHhII130_assertion description "[In this study we analyzed bone marrow and blood samples from 13 patients with myeloid leukemia (de novo myelodysplastic syndrome [MDS], n = 3; de novo acute myeloid leukemia [AML], n = 9; therapy-related (t-) AML, n = 1) which, on chromosome banding analysis, exhibited deletions (n = 12) or in one case a balanced translocation involving bands 7q31-qter using fluorescence in situ hybridization (FISH).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP913971.RArHG7anJvhmGuZd1Rzd8JGmEFTbvxMfP5OCzWrVgHhII130_provenance.
- NP913971.RArHG7anJvhmGuZd1Rzd8JGmEFTbvxMfP5OCzWrVgHhII130_assertion evidence source_evidence_literature NP913971.RArHG7anJvhmGuZd1Rzd8JGmEFTbvxMfP5OCzWrVgHhII130_provenance.
- NP913971.RArHG7anJvhmGuZd1Rzd8JGmEFTbvxMfP5OCzWrVgHhII130_assertion SIO_000772 9834205 NP913971.RArHG7anJvhmGuZd1Rzd8JGmEFTbvxMfP5OCzWrVgHhII130_provenance.
- NP913971.RArHG7anJvhmGuZd1Rzd8JGmEFTbvxMfP5OCzWrVgHhII130_assertion wasDerivedFrom befree-20150227 NP913971.RArHG7anJvhmGuZd1Rzd8JGmEFTbvxMfP5OCzWrVgHhII130_provenance.
- NP913971.RArHG7anJvhmGuZd1Rzd8JGmEFTbvxMfP5OCzWrVgHhII130_assertion wasGeneratedBy ECO_0000203 NP913971.RArHG7anJvhmGuZd1Rzd8JGmEFTbvxMfP5OCzWrVgHhII130_provenance.