Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP914128.RAELb6q5V2OAsGOG2Vi0uZahQrAw2ikBoiSATFoRFtdS0130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP914128.RAELb6q5V2OAsGOG2Vi0uZahQrAw2ikBoiSATFoRFtdS0130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP914128.RAELb6q5V2OAsGOG2Vi0uZahQrAw2ikBoiSATFoRFtdS0130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP914128.RAELb6q5V2OAsGOG2Vi0uZahQrAw2ikBoiSATFoRFtdS0130_provenance.
- NP914128.RAELb6q5V2OAsGOG2Vi0uZahQrAw2ikBoiSATFoRFtdS0130_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." NP914128.RAELb6q5V2OAsGOG2Vi0uZahQrAw2ikBoiSATFoRFtdS0130_provenance.
- NP914128.RAELb6q5V2OAsGOG2Vi0uZahQrAw2ikBoiSATFoRFtdS0130_assertion evidence source_evidence_literature NP914128.RAELb6q5V2OAsGOG2Vi0uZahQrAw2ikBoiSATFoRFtdS0130_provenance.
- NP914128.RAELb6q5V2OAsGOG2Vi0uZahQrAw2ikBoiSATFoRFtdS0130_assertion SIO_000772 11960342 NP914128.RAELb6q5V2OAsGOG2Vi0uZahQrAw2ikBoiSATFoRFtdS0130_provenance.
- NP914128.RAELb6q5V2OAsGOG2Vi0uZahQrAw2ikBoiSATFoRFtdS0130_assertion wasDerivedFrom befree-20150227 NP914128.RAELb6q5V2OAsGOG2Vi0uZahQrAw2ikBoiSATFoRFtdS0130_provenance.
- NP914128.RAELb6q5V2OAsGOG2Vi0uZahQrAw2ikBoiSATFoRFtdS0130_assertion wasGeneratedBy ECO_0000203 NP914128.RAELb6q5V2OAsGOG2Vi0uZahQrAw2ikBoiSATFoRFtdS0130_provenance.
- befree-20150227 importedOn "2015-02-27" NP914128.RAELb6q5V2OAsGOG2Vi0uZahQrAw2ikBoiSATFoRFtdS0130_provenance.