Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP883685.RAi4dfWriGm5cJGFE9p8G1L9aCeRxayXJ1McwGO9vnHtA130_assertion> ?p ?o ?g. }
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- NP883685.RAi4dfWriGm5cJGFE9p8G1L9aCeRxayXJ1McwGO9vnHtA130_assertion type Assertion NP883685.RAi4dfWriGm5cJGFE9p8G1L9aCeRxayXJ1McwGO9vnHtA130_head.
- NP883685.RAi4dfWriGm5cJGFE9p8G1L9aCeRxayXJ1McwGO9vnHtA130_assertion description "[To extend these results we searched for mutations of ASXL1 in a series of chronic myelomonocytic leukaemias, a disease classified as MDS/Myeloproliferative disorder, and found mutations in 17 out of 39 patients (43%).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP883685.RAi4dfWriGm5cJGFE9p8G1L9aCeRxayXJ1McwGO9vnHtA130_provenance.
- NP883685.RAi4dfWriGm5cJGFE9p8G1L9aCeRxayXJ1McwGO9vnHtA130_assertion evidence source_evidence_literature NP883685.RAi4dfWriGm5cJGFE9p8G1L9aCeRxayXJ1McwGO9vnHtA130_provenance.
- NP883685.RAi4dfWriGm5cJGFE9p8G1L9aCeRxayXJ1McwGO9vnHtA130_assertion SIO_000772 19388938 NP883685.RAi4dfWriGm5cJGFE9p8G1L9aCeRxayXJ1McwGO9vnHtA130_provenance.
- NP883685.RAi4dfWriGm5cJGFE9p8G1L9aCeRxayXJ1McwGO9vnHtA130_assertion wasDerivedFrom befree-20140225 NP883685.RAi4dfWriGm5cJGFE9p8G1L9aCeRxayXJ1McwGO9vnHtA130_provenance.
- NP883685.RAi4dfWriGm5cJGFE9p8G1L9aCeRxayXJ1McwGO9vnHtA130_assertion wasGeneratedBy ECO_0000203 NP883685.RAi4dfWriGm5cJGFE9p8G1L9aCeRxayXJ1McwGO9vnHtA130_provenance.