Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP685796.RA91Di0KCIHBsZbBQDvPnxtHpbMCnkSnDX8kG2GreQhhY130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP685796.RA91Di0KCIHBsZbBQDvPnxtHpbMCnkSnDX8kG2GreQhhY130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP685796.RA91Di0KCIHBsZbBQDvPnxtHpbMCnkSnDX8kG2GreQhhY130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP685796.RA91Di0KCIHBsZbBQDvPnxtHpbMCnkSnDX8kG2GreQhhY130_provenance.
- NP685796.RA91Di0KCIHBsZbBQDvPnxtHpbMCnkSnDX8kG2GreQhhY130_assertion description "[Low ERG and BAALC expression (E/B(low)) and NOTCH1/FBXW7 (N/F) mutations have been proposed as powerful prognostic markers in large cohorts of adult T-ALL.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP685796.RA91Di0KCIHBsZbBQDvPnxtHpbMCnkSnDX8kG2GreQhhY130_provenance.
- NP685796.RA91Di0KCIHBsZbBQDvPnxtHpbMCnkSnDX8kG2GreQhhY130_assertion evidence source_evidence_literature NP685796.RA91Di0KCIHBsZbBQDvPnxtHpbMCnkSnDX8kG2GreQhhY130_provenance.
- NP685796.RA91Di0KCIHBsZbBQDvPnxtHpbMCnkSnDX8kG2GreQhhY130_assertion SIO_000772 21835957 NP685796.RA91Di0KCIHBsZbBQDvPnxtHpbMCnkSnDX8kG2GreQhhY130_provenance.
- NP685796.RA91Di0KCIHBsZbBQDvPnxtHpbMCnkSnDX8kG2GreQhhY130_assertion wasDerivedFrom befree-20140225 NP685796.RA91Di0KCIHBsZbBQDvPnxtHpbMCnkSnDX8kG2GreQhhY130_provenance.
- NP685796.RA91Di0KCIHBsZbBQDvPnxtHpbMCnkSnDX8kG2GreQhhY130_assertion wasGeneratedBy ECO_0000203 NP685796.RA91Di0KCIHBsZbBQDvPnxtHpbMCnkSnDX8kG2GreQhhY130_provenance.
- befree-20140225 importedOn "2014-02-25" NP685796.RA91Di0KCIHBsZbBQDvPnxtHpbMCnkSnDX8kG2GreQhhY130_provenance.