Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP978529.RAHhOHSMJ7_RyPhtIUFJQ_0Fm-z2-rz1IWkh9XKbmND1E130_assertion> ?p ?o ?g. }
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- NP978529.RAHhOHSMJ7_RyPhtIUFJQ_0Fm-z2-rz1IWkh9XKbmND1E130_assertion type Assertion NP978529.RAHhOHSMJ7_RyPhtIUFJQ_0Fm-z2-rz1IWkh9XKbmND1E130_head.
- NP978529.RAHhOHSMJ7_RyPhtIUFJQ_0Fm-z2-rz1IWkh9XKbmND1E130_assertion description "[In particular, ASXL1 mutations are common in patients with hematologic malignancies associated with myelodysplasia, including myelodysplastic syndromes (MDSs), and chronic myelomonocytic leukemia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP978529.RAHhOHSMJ7_RyPhtIUFJQ_0Fm-z2-rz1IWkh9XKbmND1E130_provenance.
- NP978529.RAHhOHSMJ7_RyPhtIUFJQ_0Fm-z2-rz1IWkh9XKbmND1E130_assertion evidence source_evidence_literature NP978529.RAHhOHSMJ7_RyPhtIUFJQ_0Fm-z2-rz1IWkh9XKbmND1E130_provenance.
- NP978529.RAHhOHSMJ7_RyPhtIUFJQ_0Fm-z2-rz1IWkh9XKbmND1E130_assertion SIO_000772 24216483 NP978529.RAHhOHSMJ7_RyPhtIUFJQ_0Fm-z2-rz1IWkh9XKbmND1E130_provenance.
- NP978529.RAHhOHSMJ7_RyPhtIUFJQ_0Fm-z2-rz1IWkh9XKbmND1E130_assertion wasDerivedFrom befree-20150227 NP978529.RAHhOHSMJ7_RyPhtIUFJQ_0Fm-z2-rz1IWkh9XKbmND1E130_provenance.
- NP978529.RAHhOHSMJ7_RyPhtIUFJQ_0Fm-z2-rz1IWkh9XKbmND1E130_assertion wasGeneratedBy ECO_0000203 NP978529.RAHhOHSMJ7_RyPhtIUFJQ_0Fm-z2-rz1IWkh9XKbmND1E130_provenance.