Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP798416.RAv0JvrBrFvW9Po3t1ekRX79mZKoUd8e4FvjZ7j58Ou7Q130_assertion> ?p ?o ?g. }
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- NP798416.RAv0JvrBrFvW9Po3t1ekRX79mZKoUd8e4FvjZ7j58Ou7Q130_assertion type Assertion NP798416.RAv0JvrBrFvW9Po3t1ekRX79mZKoUd8e4FvjZ7j58Ou7Q130_head.
- NP798416.RAv0JvrBrFvW9Po3t1ekRX79mZKoUd8e4FvjZ7j58Ou7Q130_assertion description "[Overlaps between the diverse disorders were seen also for the JAK2V617F (MPN 66/89; 74%; MDS/MPN 4/14; 29%; MDS 2/63; 3%) and NRAS mutations (MDS 2/67; 3%; MPN 2/4; MDS/MPN 1/1).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP798416.RAv0JvrBrFvW9Po3t1ekRX79mZKoUd8e4FvjZ7j58Ou7Q130_provenance.
- NP798416.RAv0JvrBrFvW9Po3t1ekRX79mZKoUd8e4FvjZ7j58Ou7Q130_assertion evidence source_evidence_literature NP798416.RAv0JvrBrFvW9Po3t1ekRX79mZKoUd8e4FvjZ7j58Ou7Q130_provenance.
- NP798416.RAv0JvrBrFvW9Po3t1ekRX79mZKoUd8e4FvjZ7j58Ou7Q130_assertion SIO_000772 19415278 NP798416.RAv0JvrBrFvW9Po3t1ekRX79mZKoUd8e4FvjZ7j58Ou7Q130_provenance.
- NP798416.RAv0JvrBrFvW9Po3t1ekRX79mZKoUd8e4FvjZ7j58Ou7Q130_assertion wasDerivedFrom befree-20140225 NP798416.RAv0JvrBrFvW9Po3t1ekRX79mZKoUd8e4FvjZ7j58Ou7Q130_provenance.
- NP798416.RAv0JvrBrFvW9Po3t1ekRX79mZKoUd8e4FvjZ7j58Ou7Q130_assertion wasGeneratedBy ECO_0000203 NP798416.RAv0JvrBrFvW9Po3t1ekRX79mZKoUd8e4FvjZ7j58Ou7Q130_provenance.