Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP955594.RAqtiqXnNnuxS5TdsmKUC6q1I5p19ExfJZdSUPCgbbyAw130_assertion> ?p ?o ?g. }
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- NP955594.RAqtiqXnNnuxS5TdsmKUC6q1I5p19ExfJZdSUPCgbbyAw130_assertion type Assertion NP955594.RAqtiqXnNnuxS5TdsmKUC6q1I5p19ExfJZdSUPCgbbyAw130_head.
- NP955594.RAqtiqXnNnuxS5TdsmKUC6q1I5p19ExfJZdSUPCgbbyAw130_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." NP955594.RAqtiqXnNnuxS5TdsmKUC6q1I5p19ExfJZdSUPCgbbyAw130_provenance.
- NP955594.RAqtiqXnNnuxS5TdsmKUC6q1I5p19ExfJZdSUPCgbbyAw130_assertion evidence source_evidence_literature NP955594.RAqtiqXnNnuxS5TdsmKUC6q1I5p19ExfJZdSUPCgbbyAw130_provenance.
- NP955594.RAqtiqXnNnuxS5TdsmKUC6q1I5p19ExfJZdSUPCgbbyAw130_assertion SIO_000772 22271902 NP955594.RAqtiqXnNnuxS5TdsmKUC6q1I5p19ExfJZdSUPCgbbyAw130_provenance.
- NP955594.RAqtiqXnNnuxS5TdsmKUC6q1I5p19ExfJZdSUPCgbbyAw130_assertion wasDerivedFrom befree-2016 NP955594.RAqtiqXnNnuxS5TdsmKUC6q1I5p19ExfJZdSUPCgbbyAw130_provenance.
- NP955594.RAqtiqXnNnuxS5TdsmKUC6q1I5p19ExfJZdSUPCgbbyAw130_assertion wasGeneratedBy ECO_0000203 NP955594.RAqtiqXnNnuxS5TdsmKUC6q1I5p19ExfJZdSUPCgbbyAw130_provenance.