Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP7598.RA-Ql2hrygJDC8DX3L212u8113CkxTVP-iXnCuyyD3mQk130_assertion> ?p ?o ?g. }
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- NP7598.RA-Ql2hrygJDC8DX3L212u8113CkxTVP-iXnCuyyD3mQk130_assertion type Assertion NP7598.RA-Ql2hrygJDC8DX3L212u8113CkxTVP-iXnCuyyD3mQk130_head.
- NP7598.RA-Ql2hrygJDC8DX3L212u8113CkxTVP-iXnCuyyD3mQk130_assertion description "[Mutations in SETBP1 are recurrent in myelodysplastic syndromes and often coexist with cytogenetic markers associated with disease progression.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP7598.RA-Ql2hrygJDC8DX3L212u8113CkxTVP-iXnCuyyD3mQk130_provenance.
- NP7598.RA-Ql2hrygJDC8DX3L212u8113CkxTVP-iXnCuyyD3mQk130_assertion evidence source_evidence_curated NP7598.RA-Ql2hrygJDC8DX3L212u8113CkxTVP-iXnCuyyD3mQk130_provenance.
- NP7598.RA-Ql2hrygJDC8DX3L212u8113CkxTVP-iXnCuyyD3mQk130_assertion SIO_000772 23889083 NP7598.RA-Ql2hrygJDC8DX3L212u8113CkxTVP-iXnCuyyD3mQk130_provenance.
- NP7598.RA-Ql2hrygJDC8DX3L212u8113CkxTVP-iXnCuyyD3mQk130_assertion wasDerivedFrom uniprot-2016 NP7598.RA-Ql2hrygJDC8DX3L212u8113CkxTVP-iXnCuyyD3mQk130_provenance.
- NP7598.RA-Ql2hrygJDC8DX3L212u8113CkxTVP-iXnCuyyD3mQk130_assertion wasGeneratedBy ECO_0000218 NP7598.RA-Ql2hrygJDC8DX3L212u8113CkxTVP-iXnCuyyD3mQk130_provenance.