Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP176876.RA6YmtYrnZuYu0A-e7dOgCckhfKlVz_ZCYAjsRjlY0Glg130_assertion> ?p ?o ?g. }
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- NP176876.RA6YmtYrnZuYu0A-e7dOgCckhfKlVz_ZCYAjsRjlY0Glg130_assertion type Assertion NP176876.RA6YmtYrnZuYu0A-e7dOgCckhfKlVz_ZCYAjsRjlY0Glg130_head.
- NP176876.RA6YmtYrnZuYu0A-e7dOgCckhfKlVz_ZCYAjsRjlY0Glg130_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." NP176876.RA6YmtYrnZuYu0A-e7dOgCckhfKlVz_ZCYAjsRjlY0Glg130_provenance.
- NP176876.RA6YmtYrnZuYu0A-e7dOgCckhfKlVz_ZCYAjsRjlY0Glg130_assertion evidence source_evidence_literature NP176876.RA6YmtYrnZuYu0A-e7dOgCckhfKlVz_ZCYAjsRjlY0Glg130_provenance.
- NP176876.RA6YmtYrnZuYu0A-e7dOgCckhfKlVz_ZCYAjsRjlY0Glg130_assertion SIO_000772 20494930 NP176876.RA6YmtYrnZuYu0A-e7dOgCckhfKlVz_ZCYAjsRjlY0Glg130_provenance.
- NP176876.RA6YmtYrnZuYu0A-e7dOgCckhfKlVz_ZCYAjsRjlY0Glg130_assertion wasDerivedFrom gad-20150221 NP176876.RA6YmtYrnZuYu0A-e7dOgCckhfKlVz_ZCYAjsRjlY0Glg130_provenance.
- NP176876.RA6YmtYrnZuYu0A-e7dOgCckhfKlVz_ZCYAjsRjlY0Glg130_assertion wasGeneratedBy ECO_0000203 NP176876.RA6YmtYrnZuYu0A-e7dOgCckhfKlVz_ZCYAjsRjlY0Glg130_provenance.