Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP474917.RAIK4nhOAZcSzC6Bjfor9FN57vHhhzJqnqFQG4nXSJZVc130_assertion> ?p ?o ?g. }
Showing items 1 to 6 of
6
with 100 items per page.
- NP474917.RAIK4nhOAZcSzC6Bjfor9FN57vHhhzJqnqFQG4nXSJZVc130_assertion type Assertion NP474917.RAIK4nhOAZcSzC6Bjfor9FN57vHhhzJqnqFQG4nXSJZVc130_head.
- NP474917.RAIK4nhOAZcSzC6Bjfor9FN57vHhhzJqnqFQG4nXSJZVc130_assertion description "[We have studied the mutational status of TET2 (complete coding region), ASXL1 (exon12), IDH1 (R132), IDH2 (R140 and R172), and c-CBL (exons 8 and 9) in 62 MPN patients (52 essential thrombocythemia (ET), five polycythemia vera (PV), and five primary myelofibrosis (PMF)) negative for both JAK2 (V617F and exon 12) and MPL (exon 10) mutations.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP474917.RAIK4nhOAZcSzC6Bjfor9FN57vHhhzJqnqFQG4nXSJZVc130_provenance.
- NP474917.RAIK4nhOAZcSzC6Bjfor9FN57vHhhzJqnqFQG4nXSJZVc130_assertion evidence source_evidence_literature NP474917.RAIK4nhOAZcSzC6Bjfor9FN57vHhhzJqnqFQG4nXSJZVc130_provenance.
- NP474917.RAIK4nhOAZcSzC6Bjfor9FN57vHhhzJqnqFQG4nXSJZVc130_assertion SIO_000772 21904853 NP474917.RAIK4nhOAZcSzC6Bjfor9FN57vHhhzJqnqFQG4nXSJZVc130_provenance.
- NP474917.RAIK4nhOAZcSzC6Bjfor9FN57vHhhzJqnqFQG4nXSJZVc130_assertion wasDerivedFrom befree-20150227 NP474917.RAIK4nhOAZcSzC6Bjfor9FN57vHhhzJqnqFQG4nXSJZVc130_provenance.
- NP474917.RAIK4nhOAZcSzC6Bjfor9FN57vHhhzJqnqFQG4nXSJZVc130_assertion wasGeneratedBy ECO_0000203 NP474917.RAIK4nhOAZcSzC6Bjfor9FN57vHhhzJqnqFQG4nXSJZVc130_provenance.