Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP125688.RA6ipIRF4Nb2kSdGsWsiYe_38dFYVVcv_uTIZb0zeh5wg130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP125688.RA6ipIRF4Nb2kSdGsWsiYe_38dFYVVcv_uTIZb0zeh5wg130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP125688.RA6ipIRF4Nb2kSdGsWsiYe_38dFYVVcv_uTIZb0zeh5wg130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP125688.RA6ipIRF4Nb2kSdGsWsiYe_38dFYVVcv_uTIZb0zeh5wg130_provenance.
- NP125688.RA6ipIRF4Nb2kSdGsWsiYe_38dFYVVcv_uTIZb0zeh5wg130_assertion description "[Five SNPs (BLM rs441399, RAD50 rs2237060, FAM82A2 rs2304583, ERCC3 rs4150506, and XRCC4 rs13178127) were particularly noteworthy because their gene regions were significantly associated with NHL or NHL subtypes (minP a$? 0A*05), or because of high level of statistical significance (P a$? 0A*005) and consistent findings across the three studies.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP125688.RA6ipIRF4Nb2kSdGsWsiYe_38dFYVVcv_uTIZb0zeh5wg130_provenance.
- NP125688.RA6ipIRF4Nb2kSdGsWsiYe_38dFYVVcv_uTIZb0zeh5wg130_assertion evidence source_evidence_literature NP125688.RA6ipIRF4Nb2kSdGsWsiYe_38dFYVVcv_uTIZb0zeh5wg130_provenance.
- NP125688.RA6ipIRF4Nb2kSdGsWsiYe_38dFYVVcv_uTIZb0zeh5wg130_assertion SIO_000772 20813000 NP125688.RA6ipIRF4Nb2kSdGsWsiYe_38dFYVVcv_uTIZb0zeh5wg130_provenance.
- NP125688.RA6ipIRF4Nb2kSdGsWsiYe_38dFYVVcv_uTIZb0zeh5wg130_assertion wasDerivedFrom gad-20150221 NP125688.RA6ipIRF4Nb2kSdGsWsiYe_38dFYVVcv_uTIZb0zeh5wg130_provenance.
- NP125688.RA6ipIRF4Nb2kSdGsWsiYe_38dFYVVcv_uTIZb0zeh5wg130_assertion wasGeneratedBy ECO_0000203 NP125688.RA6ipIRF4Nb2kSdGsWsiYe_38dFYVVcv_uTIZb0zeh5wg130_provenance.
- gad-20150221 importedOn "2015-02-21" NP125688.RA6ipIRF4Nb2kSdGsWsiYe_38dFYVVcv_uTIZb0zeh5wg130_provenance.