Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP826556.RAO8TA3V8maI85A2IxYLY0QAJGt5_5bUSHt2AKmhvSGlI130_assertion> ?p ?o ?g. }
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- NP826556.RAO8TA3V8maI85A2IxYLY0QAJGt5_5bUSHt2AKmhvSGlI130_assertion type Assertion NP826556.RAO8TA3V8maI85A2IxYLY0QAJGt5_5bUSHt2AKmhvSGlI130_head.
- NP826556.RAO8TA3V8maI85A2IxYLY0QAJGt5_5bUSHt2AKmhvSGlI130_assertion description "[We, therefore, investigated individuals from families with one or more first-degree relatives with myelodysplastic syndrome/acute myeloid leukemia with wild-type RUNX1 and CEBPA, for GATA2 mutations.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP826556.RAO8TA3V8maI85A2IxYLY0QAJGt5_5bUSHt2AKmhvSGlI130_provenance.
- NP826556.RAO8TA3V8maI85A2IxYLY0QAJGt5_5bUSHt2AKmhvSGlI130_assertion evidence source_evidence_literature NP826556.RAO8TA3V8maI85A2IxYLY0QAJGt5_5bUSHt2AKmhvSGlI130_provenance.
- NP826556.RAO8TA3V8maI85A2IxYLY0QAJGt5_5bUSHt2AKmhvSGlI130_assertion SIO_000772 22271902 NP826556.RAO8TA3V8maI85A2IxYLY0QAJGt5_5bUSHt2AKmhvSGlI130_provenance.
- NP826556.RAO8TA3V8maI85A2IxYLY0QAJGt5_5bUSHt2AKmhvSGlI130_assertion wasDerivedFrom befree-20140225 NP826556.RAO8TA3V8maI85A2IxYLY0QAJGt5_5bUSHt2AKmhvSGlI130_provenance.
- NP826556.RAO8TA3V8maI85A2IxYLY0QAJGt5_5bUSHt2AKmhvSGlI130_assertion wasGeneratedBy ECO_0000203 NP826556.RAO8TA3V8maI85A2IxYLY0QAJGt5_5bUSHt2AKmhvSGlI130_provenance.