Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP635592.RA_jIehEF0EXgIlWoktkbGKXhyvMlfGYpLcb6lYnUH4fM130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP635592.RA_jIehEF0EXgIlWoktkbGKXhyvMlfGYpLcb6lYnUH4fM130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP635592.RA_jIehEF0EXgIlWoktkbGKXhyvMlfGYpLcb6lYnUH4fM130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP635592.RA_jIehEF0EXgIlWoktkbGKXhyvMlfGYpLcb6lYnUH4fM130_provenance.
- NP635592.RA_jIehEF0EXgIlWoktkbGKXhyvMlfGYpLcb6lYnUH4fM130_assertion description "[Here we report that the protein encoded by the BTG1 gene, which is frequently deleted in (pediatric) ALL, is a key determinant of GC responsiveness.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP635592.RA_jIehEF0EXgIlWoktkbGKXhyvMlfGYpLcb6lYnUH4fM130_provenance.
- NP635592.RA_jIehEF0EXgIlWoktkbGKXhyvMlfGYpLcb6lYnUH4fM130_assertion evidence source_evidence_literature NP635592.RA_jIehEF0EXgIlWoktkbGKXhyvMlfGYpLcb6lYnUH4fM130_provenance.
- NP635592.RA_jIehEF0EXgIlWoktkbGKXhyvMlfGYpLcb6lYnUH4fM130_assertion SIO_000772 20354172 NP635592.RA_jIehEF0EXgIlWoktkbGKXhyvMlfGYpLcb6lYnUH4fM130_provenance.
- NP635592.RA_jIehEF0EXgIlWoktkbGKXhyvMlfGYpLcb6lYnUH4fM130_assertion wasDerivedFrom befree-20140225 NP635592.RA_jIehEF0EXgIlWoktkbGKXhyvMlfGYpLcb6lYnUH4fM130_provenance.
- NP635592.RA_jIehEF0EXgIlWoktkbGKXhyvMlfGYpLcb6lYnUH4fM130_assertion wasGeneratedBy ECO_0000203 NP635592.RA_jIehEF0EXgIlWoktkbGKXhyvMlfGYpLcb6lYnUH4fM130_provenance.
- befree-20140225 importedOn "2014-02-25" NP635592.RA_jIehEF0EXgIlWoktkbGKXhyvMlfGYpLcb6lYnUH4fM130_provenance.