Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP561364.RAnXPNDQ3Jd6eXuSu0xC9HKuN-YZRMDCaqWc75dPk_3sc130_assertion> ?p ?o ?g. }
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- NP561364.RAnXPNDQ3Jd6eXuSu0xC9HKuN-YZRMDCaqWc75dPk_3sc130_assertion type Assertion NP561364.RAnXPNDQ3Jd6eXuSu0xC9HKuN-YZRMDCaqWc75dPk_3sc130_head.
- NP561364.RAnXPNDQ3Jd6eXuSu0xC9HKuN-YZRMDCaqWc75dPk_3sc130_assertion description "[In particular, ASXL1 mutations are common in patients with hematologic malignancies associated with myelodysplasia, including myelodysplastic syndromes (MDSs), and chronic myelomonocytic leukemia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP561364.RAnXPNDQ3Jd6eXuSu0xC9HKuN-YZRMDCaqWc75dPk_3sc130_provenance.
- NP561364.RAnXPNDQ3Jd6eXuSu0xC9HKuN-YZRMDCaqWc75dPk_3sc130_assertion evidence source_evidence_literature NP561364.RAnXPNDQ3Jd6eXuSu0xC9HKuN-YZRMDCaqWc75dPk_3sc130_provenance.
- NP561364.RAnXPNDQ3Jd6eXuSu0xC9HKuN-YZRMDCaqWc75dPk_3sc130_assertion SIO_000772 24216483 NP561364.RAnXPNDQ3Jd6eXuSu0xC9HKuN-YZRMDCaqWc75dPk_3sc130_provenance.
- NP561364.RAnXPNDQ3Jd6eXuSu0xC9HKuN-YZRMDCaqWc75dPk_3sc130_assertion wasDerivedFrom befree-20140225 NP561364.RAnXPNDQ3Jd6eXuSu0xC9HKuN-YZRMDCaqWc75dPk_3sc130_provenance.
- NP561364.RAnXPNDQ3Jd6eXuSu0xC9HKuN-YZRMDCaqWc75dPk_3sc130_assertion wasGeneratedBy ECO_0000203 NP561364.RAnXPNDQ3Jd6eXuSu0xC9HKuN-YZRMDCaqWc75dPk_3sc130_provenance.