Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP136155.RA7FyV9KgXBQ3GCts0b_xDldNJwAntVjUd-CN6BCIyJ9E130_assertion> ?p ?o ?g. }
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- NP136155.RA7FyV9KgXBQ3GCts0b_xDldNJwAntVjUd-CN6BCIyJ9E130_assertion type Assertion NP136155.RA7FyV9KgXBQ3GCts0b_xDldNJwAntVjUd-CN6BCIyJ9E130_head.
- NP136155.RA7FyV9KgXBQ3GCts0b_xDldNJwAntVjUd-CN6BCIyJ9E130_assertion description "[These results suggest that IDH1 mutations are recurrent molecular aberrations in patients with myelodysplastic syndromes, and may become useful as a poor risk marker in these patients. These findings await validation in prospective trials.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP136155.RA7FyV9KgXBQ3GCts0b_xDldNJwAntVjUd-CN6BCIyJ9E130_provenance.
- NP136155.RA7FyV9KgXBQ3GCts0b_xDldNJwAntVjUd-CN6BCIyJ9E130_assertion evidence source_evidence_literature NP136155.RA7FyV9KgXBQ3GCts0b_xDldNJwAntVjUd-CN6BCIyJ9E130_provenance.
- NP136155.RA7FyV9KgXBQ3GCts0b_xDldNJwAntVjUd-CN6BCIyJ9E130_assertion SIO_000772 20494930 NP136155.RA7FyV9KgXBQ3GCts0b_xDldNJwAntVjUd-CN6BCIyJ9E130_provenance.
- NP136155.RA7FyV9KgXBQ3GCts0b_xDldNJwAntVjUd-CN6BCIyJ9E130_assertion wasDerivedFrom gad-20150221 NP136155.RA7FyV9KgXBQ3GCts0b_xDldNJwAntVjUd-CN6BCIyJ9E130_provenance.
- NP136155.RA7FyV9KgXBQ3GCts0b_xDldNJwAntVjUd-CN6BCIyJ9E130_assertion wasGeneratedBy ECO_0000203 NP136155.RA7FyV9KgXBQ3GCts0b_xDldNJwAntVjUd-CN6BCIyJ9E130_provenance.