Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP844298.RAEMKgjfNA6auoJVNj2JKmld7IZuDkRw2vaaacniamZ5A130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP844298.RAEMKgjfNA6auoJVNj2JKmld7IZuDkRw2vaaacniamZ5A130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP844298.RAEMKgjfNA6auoJVNj2JKmld7IZuDkRw2vaaacniamZ5A130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP844298.RAEMKgjfNA6auoJVNj2JKmld7IZuDkRw2vaaacniamZ5A130_provenance.
- NP844298.RAEMKgjfNA6auoJVNj2JKmld7IZuDkRw2vaaacniamZ5A130_assertion description "[We used the allelic discrimination method to identify polymorphisms in GSTT1, SULT1C2, CDA, SXR (drug metabolic pathways), XPD, XPA, XPG, ERCC1, TOP2A (DNA repair), VEGF (angiogenesis), and MDR1 (multidrug resistance) genes in 110 adult patients with intermediate-risk AML, enrolled in the CETLAM-99 prospective trial.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP844298.RAEMKgjfNA6auoJVNj2JKmld7IZuDkRw2vaaacniamZ5A130_provenance.
- NP844298.RAEMKgjfNA6auoJVNj2JKmld7IZuDkRw2vaaacniamZ5A130_assertion evidence source_evidence_literature NP844298.RAEMKgjfNA6auoJVNj2JKmld7IZuDkRw2vaaacniamZ5A130_provenance.
- NP844298.RAEMKgjfNA6auoJVNj2JKmld7IZuDkRw2vaaacniamZ5A130_assertion SIO_000772 16507781 NP844298.RAEMKgjfNA6auoJVNj2JKmld7IZuDkRw2vaaacniamZ5A130_provenance.
- NP844298.RAEMKgjfNA6auoJVNj2JKmld7IZuDkRw2vaaacniamZ5A130_assertion wasDerivedFrom befree-20140225 NP844298.RAEMKgjfNA6auoJVNj2JKmld7IZuDkRw2vaaacniamZ5A130_provenance.
- NP844298.RAEMKgjfNA6auoJVNj2JKmld7IZuDkRw2vaaacniamZ5A130_assertion wasGeneratedBy ECO_0000203 NP844298.RAEMKgjfNA6auoJVNj2JKmld7IZuDkRw2vaaacniamZ5A130_provenance.
- befree-20140225 importedOn "2014-02-25" NP844298.RAEMKgjfNA6auoJVNj2JKmld7IZuDkRw2vaaacniamZ5A130_provenance.