Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP99518.RAhFpPS3xNaPUSx_Sl6RpAW-smCQx-dwovkDZ4Xf78cmo130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP99518.RAhFpPS3xNaPUSx_Sl6RpAW-smCQx-dwovkDZ4Xf78cmo130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP99518.RAhFpPS3xNaPUSx_Sl6RpAW-smCQx-dwovkDZ4Xf78cmo130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP99518.RAhFpPS3xNaPUSx_Sl6RpAW-smCQx-dwovkDZ4Xf78cmo130_provenance.
- NP99518.RAhFpPS3xNaPUSx_Sl6RpAW-smCQx-dwovkDZ4Xf78cmo130_assertion description "[The XRCC1 399Gln allele was associated with a reduction of risk of high-risk adenomas (OR 0.62, 95% CI 0.41-0.96).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP99518.RAhFpPS3xNaPUSx_Sl6RpAW-smCQx-dwovkDZ4Xf78cmo130_provenance.
- NP99518.RAhFpPS3xNaPUSx_Sl6RpAW-smCQx-dwovkDZ4Xf78cmo130_assertion evidence source_evidence_literature NP99518.RAhFpPS3xNaPUSx_Sl6RpAW-smCQx-dwovkDZ4Xf78cmo130_provenance.
- NP99518.RAhFpPS3xNaPUSx_Sl6RpAW-smCQx-dwovkDZ4Xf78cmo130_assertion SIO_000772 16542436 NP99518.RAhFpPS3xNaPUSx_Sl6RpAW-smCQx-dwovkDZ4Xf78cmo130_provenance.
- NP99518.RAhFpPS3xNaPUSx_Sl6RpAW-smCQx-dwovkDZ4Xf78cmo130_assertion wasDerivedFrom gad-20150221 NP99518.RAhFpPS3xNaPUSx_Sl6RpAW-smCQx-dwovkDZ4Xf78cmo130_provenance.
- NP99518.RAhFpPS3xNaPUSx_Sl6RpAW-smCQx-dwovkDZ4Xf78cmo130_assertion wasGeneratedBy ECO_0000203 NP99518.RAhFpPS3xNaPUSx_Sl6RpAW-smCQx-dwovkDZ4Xf78cmo130_provenance.
- gad-20150221 importedOn "2015-02-21" NP99518.RAhFpPS3xNaPUSx_Sl6RpAW-smCQx-dwovkDZ4Xf78cmo130_provenance.