Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP399553.RAAQf8Rt6edOITWDL1tcuzuq310ImCs6BEnESB1sTLDVQ130_assertion> ?p ?o ?g. }
Showing items 1 to 6 of
6
with 100 items per page.
- NP399553.RAAQf8Rt6edOITWDL1tcuzuq310ImCs6BEnESB1sTLDVQ130_assertion type Assertion NP399553.RAAQf8Rt6edOITWDL1tcuzuq310ImCs6BEnESB1sTLDVQ130_head.
- NP399553.RAAQf8Rt6edOITWDL1tcuzuq310ImCs6BEnESB1sTLDVQ130_assertion description "[Cryptic and partial deletions of PRDM16 and RUNX1 without t(1;21)(p36;q22) and/or RUNX1-PRDM16 fusion in a case of progressive chronic myeloid leukemia: a complex chromosomal rearrangement of underestimated frequency in disease progression?]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP399553.RAAQf8Rt6edOITWDL1tcuzuq310ImCs6BEnESB1sTLDVQ130_provenance.
- NP399553.RAAQf8Rt6edOITWDL1tcuzuq310ImCs6BEnESB1sTLDVQ130_assertion evidence source_evidence_literature NP399553.RAAQf8Rt6edOITWDL1tcuzuq310ImCs6BEnESB1sTLDVQ130_provenance.
- NP399553.RAAQf8Rt6edOITWDL1tcuzuq310ImCs6BEnESB1sTLDVQ130_assertion SIO_000772 18767145 NP399553.RAAQf8Rt6edOITWDL1tcuzuq310ImCs6BEnESB1sTLDVQ130_provenance.
- NP399553.RAAQf8Rt6edOITWDL1tcuzuq310ImCs6BEnESB1sTLDVQ130_assertion wasDerivedFrom befree-20140225 NP399553.RAAQf8Rt6edOITWDL1tcuzuq310ImCs6BEnESB1sTLDVQ130_provenance.
- NP399553.RAAQf8Rt6edOITWDL1tcuzuq310ImCs6BEnESB1sTLDVQ130_assertion wasGeneratedBy ECO_0000203 NP399553.RAAQf8Rt6edOITWDL1tcuzuq310ImCs6BEnESB1sTLDVQ130_provenance.