Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP114502.RAn01pd7qEci6vCzYnlR56NuRYbS6DyIQrpKWGm4_O1dU130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP114502.RAn01pd7qEci6vCzYnlR56NuRYbS6DyIQrpKWGm4_O1dU130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP114502.RAn01pd7qEci6vCzYnlR56NuRYbS6DyIQrpKWGm4_O1dU130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP114502.RAn01pd7qEci6vCzYnlR56NuRYbS6DyIQrpKWGm4_O1dU130_provenance.
- gad-20150221 importedOn "2015-02-21" NP114502.RAn01pd7qEci6vCzYnlR56NuRYbS6DyIQrpKWGm4_O1dU130_provenance.
- NP114502.RAn01pd7qEci6vCzYnlR56NuRYbS6DyIQrpKWGm4_O1dU130_assertion wasGeneratedBy ECO_0000203 NP114502.RAn01pd7qEci6vCzYnlR56NuRYbS6DyIQrpKWGm4_O1dU130_provenance.
- NP114502.RAn01pd7qEci6vCzYnlR56NuRYbS6DyIQrpKWGm4_O1dU130_assertion wasDerivedFrom gad-20150221 NP114502.RAn01pd7qEci6vCzYnlR56NuRYbS6DyIQrpKWGm4_O1dU130_provenance.
- NP114502.RAn01pd7qEci6vCzYnlR56NuRYbS6DyIQrpKWGm4_O1dU130_assertion SIO_000772 17959715 NP114502.RAn01pd7qEci6vCzYnlR56NuRYbS6DyIQrpKWGm4_O1dU130_provenance.
- NP114502.RAn01pd7qEci6vCzYnlR56NuRYbS6DyIQrpKWGm4_O1dU130_assertion evidence source_evidence_literature NP114502.RAn01pd7qEci6vCzYnlR56NuRYbS6DyIQrpKWGm4_O1dU130_provenance.
- NP114502.RAn01pd7qEci6vCzYnlR56NuRYbS6DyIQrpKWGm4_O1dU130_assertion description "[The MLH1 -93 variant allele was also over-represented in t-AML cases when compared to de novo AML cases (36.9%, n = 420) and healthy controls (36.3%, n = 952), and was associated with a significantly increased risk of developing t-AML (odds ratio 5.31, 95% confidence interval 1.40 to 20.15), but only in patients previously treated with a methylating agent.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP114502.RAn01pd7qEci6vCzYnlR56NuRYbS6DyIQrpKWGm4_O1dU130_provenance.