Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP176876.RA6YmtYrnZuYu0A-e7dOgCckhfKlVz_ZCYAjsRjlY0Glg130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP176876.RA6YmtYrnZuYu0A-e7dOgCckhfKlVz_ZCYAjsRjlY0Glg130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP176876.RA6YmtYrnZuYu0A-e7dOgCckhfKlVz_ZCYAjsRjlY0Glg130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP176876.RA6YmtYrnZuYu0A-e7dOgCckhfKlVz_ZCYAjsRjlY0Glg130_provenance.
- 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.
- gad-20150221 importedOn "2015-02-21" NP176876.RA6YmtYrnZuYu0A-e7dOgCckhfKlVz_ZCYAjsRjlY0Glg130_provenance.