Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP978562.RA9wIzjg7MDwVprIoKw7UOjcNFD94ZjL6iWPqlKZRtIek130_assertion> ?p ?o ?g. }
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- NP978562.RA9wIzjg7MDwVprIoKw7UOjcNFD94ZjL6iWPqlKZRtIek130_assertion type Assertion NP978562.RA9wIzjg7MDwVprIoKw7UOjcNFD94ZjL6iWPqlKZRtIek130_head.
- NP978562.RA9wIzjg7MDwVprIoKw7UOjcNFD94ZjL6iWPqlKZRtIek130_assertion description "[We found a high incidence of ASXL1 mutation in MF patients (20%) and a low incidence in PV (7%) and ET (4%) patients.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP978562.RA9wIzjg7MDwVprIoKw7UOjcNFD94ZjL6iWPqlKZRtIek130_provenance.
- NP978562.RA9wIzjg7MDwVprIoKw7UOjcNFD94ZjL6iWPqlKZRtIek130_assertion evidence source_evidence_literature NP978562.RA9wIzjg7MDwVprIoKw7UOjcNFD94ZjL6iWPqlKZRtIek130_provenance.
- NP978562.RA9wIzjg7MDwVprIoKw7UOjcNFD94ZjL6iWPqlKZRtIek130_assertion SIO_000772 22489043 NP978562.RA9wIzjg7MDwVprIoKw7UOjcNFD94ZjL6iWPqlKZRtIek130_provenance.
- NP978562.RA9wIzjg7MDwVprIoKw7UOjcNFD94ZjL6iWPqlKZRtIek130_assertion wasDerivedFrom befree-20150227 NP978562.RA9wIzjg7MDwVprIoKw7UOjcNFD94ZjL6iWPqlKZRtIek130_provenance.
- NP978562.RA9wIzjg7MDwVprIoKw7UOjcNFD94ZjL6iWPqlKZRtIek130_assertion wasGeneratedBy ECO_0000203 NP978562.RA9wIzjg7MDwVprIoKw7UOjcNFD94ZjL6iWPqlKZRtIek130_provenance.