Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP402959.RA6yF94G9ETfw1PuVh9rmP1U7ISnLHKPAxor4zgQYR2UE130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP402959.RA6yF94G9ETfw1PuVh9rmP1U7ISnLHKPAxor4zgQYR2UE130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP402959.RA6yF94G9ETfw1PuVh9rmP1U7ISnLHKPAxor4zgQYR2UE130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP402959.RA6yF94G9ETfw1PuVh9rmP1U7ISnLHKPAxor4zgQYR2UE130_provenance.
- NP402959.RA6yF94G9ETfw1PuVh9rmP1U7ISnLHKPAxor4zgQYR2UE130_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." NP402959.RA6yF94G9ETfw1PuVh9rmP1U7ISnLHKPAxor4zgQYR2UE130_provenance.
- NP402959.RA6yF94G9ETfw1PuVh9rmP1U7ISnLHKPAxor4zgQYR2UE130_assertion evidence source_evidence_literature NP402959.RA6yF94G9ETfw1PuVh9rmP1U7ISnLHKPAxor4zgQYR2UE130_provenance.
- NP402959.RA6yF94G9ETfw1PuVh9rmP1U7ISnLHKPAxor4zgQYR2UE130_assertion SIO_000772 16507781 NP402959.RA6yF94G9ETfw1PuVh9rmP1U7ISnLHKPAxor4zgQYR2UE130_provenance.
- NP402959.RA6yF94G9ETfw1PuVh9rmP1U7ISnLHKPAxor4zgQYR2UE130_assertion wasDerivedFrom befree-20140225 NP402959.RA6yF94G9ETfw1PuVh9rmP1U7ISnLHKPAxor4zgQYR2UE130_provenance.
- NP402959.RA6yF94G9ETfw1PuVh9rmP1U7ISnLHKPAxor4zgQYR2UE130_assertion wasGeneratedBy ECO_0000203 NP402959.RA6yF94G9ETfw1PuVh9rmP1U7ISnLHKPAxor4zgQYR2UE130_provenance.
- befree-20140225 importedOn "2014-02-25" NP402959.RA6yF94G9ETfw1PuVh9rmP1U7ISnLHKPAxor4zgQYR2UE130_provenance.