Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP955596.RADiC0sUd3HbLWTGChVt1CmSbB6oBX88G4ME4OVim7rKc130_assertion> ?p ?o ?g. }
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- NP955596.RADiC0sUd3HbLWTGChVt1CmSbB6oBX88G4ME4OVim7rKc130_assertion type Assertion NP955596.RADiC0sUd3HbLWTGChVt1CmSbB6oBX88G4ME4OVim7rKc130_head.
- NP955596.RADiC0sUd3HbLWTGChVt1CmSbB6oBX88G4ME4OVim7rKc130_assertion description "[Germ-line GATA2 p.THR354MET mutation in familial myelodysplastic syndrome with acquired monosomy 7 and ASXL1 mutation demonstrating rapid onset and poor survival.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP955596.RADiC0sUd3HbLWTGChVt1CmSbB6oBX88G4ME4OVim7rKc130_provenance.
- NP955596.RADiC0sUd3HbLWTGChVt1CmSbB6oBX88G4ME4OVim7rKc130_assertion evidence source_evidence_literature NP955596.RADiC0sUd3HbLWTGChVt1CmSbB6oBX88G4ME4OVim7rKc130_provenance.
- NP955596.RADiC0sUd3HbLWTGChVt1CmSbB6oBX88G4ME4OVim7rKc130_assertion SIO_000772 22271902 NP955596.RADiC0sUd3HbLWTGChVt1CmSbB6oBX88G4ME4OVim7rKc130_provenance.
- NP955596.RADiC0sUd3HbLWTGChVt1CmSbB6oBX88G4ME4OVim7rKc130_assertion wasDerivedFrom befree-2016 NP955596.RADiC0sUd3HbLWTGChVt1CmSbB6oBX88G4ME4OVim7rKc130_provenance.
- NP955596.RADiC0sUd3HbLWTGChVt1CmSbB6oBX88G4ME4OVim7rKc130_assertion wasGeneratedBy ECO_0000203 NP955596.RADiC0sUd3HbLWTGChVt1CmSbB6oBX88G4ME4OVim7rKc130_provenance.