Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP352278.RAYvox_fcMhjbjSwflz2_lIFU_zlSL9jZs_RirVlEbDFM130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP352278.RAYvox_fcMhjbjSwflz2_lIFU_zlSL9jZs_RirVlEbDFM130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP352278.RAYvox_fcMhjbjSwflz2_lIFU_zlSL9jZs_RirVlEbDFM130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP352278.RAYvox_fcMhjbjSwflz2_lIFU_zlSL9jZs_RirVlEbDFM130_provenance.
- NP352278.RAYvox_fcMhjbjSwflz2_lIFU_zlSL9jZs_RirVlEbDFM130_assertion description "[In each category except for RARS, approximately half of the patients progressed, with a slightly less median time to progression in RAEB-T than for the other subtypes of MDS.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP352278.RAYvox_fcMhjbjSwflz2_lIFU_zlSL9jZs_RirVlEbDFM130_provenance.
- NP352278.RAYvox_fcMhjbjSwflz2_lIFU_zlSL9jZs_RirVlEbDFM130_assertion evidence source_evidence_literature NP352278.RAYvox_fcMhjbjSwflz2_lIFU_zlSL9jZs_RirVlEbDFM130_provenance.
- NP352278.RAYvox_fcMhjbjSwflz2_lIFU_zlSL9jZs_RirVlEbDFM130_assertion SIO_000772 11960342 NP352278.RAYvox_fcMhjbjSwflz2_lIFU_zlSL9jZs_RirVlEbDFM130_provenance.
- NP352278.RAYvox_fcMhjbjSwflz2_lIFU_zlSL9jZs_RirVlEbDFM130_assertion wasDerivedFrom befree-2016 NP352278.RAYvox_fcMhjbjSwflz2_lIFU_zlSL9jZs_RirVlEbDFM130_provenance.
- NP352278.RAYvox_fcMhjbjSwflz2_lIFU_zlSL9jZs_RirVlEbDFM130_assertion wasGeneratedBy ECO_0000203 NP352278.RAYvox_fcMhjbjSwflz2_lIFU_zlSL9jZs_RirVlEbDFM130_provenance.
- befree-2016 importedOn "2016-02-19" NP352278.RAYvox_fcMhjbjSwflz2_lIFU_zlSL9jZs_RirVlEbDFM130_provenance.