Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP259187.RALLVhSuDRESoH9-mhe2IDWmV-moFXlqpe5LL_RKv2jc4130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP259187.RALLVhSuDRESoH9-mhe2IDWmV-moFXlqpe5LL_RKv2jc4130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP259187.RALLVhSuDRESoH9-mhe2IDWmV-moFXlqpe5LL_RKv2jc4130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP259187.RALLVhSuDRESoH9-mhe2IDWmV-moFXlqpe5LL_RKv2jc4130_provenance.
- befree-20150227 importedOn "2015-02-27" NP259187.RALLVhSuDRESoH9-mhe2IDWmV-moFXlqpe5LL_RKv2jc4130_provenance.
- NP259187.RALLVhSuDRESoH9-mhe2IDWmV-moFXlqpe5LL_RKv2jc4130_assertion wasGeneratedBy ECO_0000203 NP259187.RALLVhSuDRESoH9-mhe2IDWmV-moFXlqpe5LL_RKv2jc4130_provenance.
- NP259187.RALLVhSuDRESoH9-mhe2IDWmV-moFXlqpe5LL_RKv2jc4130_assertion wasDerivedFrom befree-20150227 NP259187.RALLVhSuDRESoH9-mhe2IDWmV-moFXlqpe5LL_RKv2jc4130_provenance.
- NP259187.RALLVhSuDRESoH9-mhe2IDWmV-moFXlqpe5LL_RKv2jc4130_assertion SIO_000772 21436895 NP259187.RALLVhSuDRESoH9-mhe2IDWmV-moFXlqpe5LL_RKv2jc4130_provenance.
- NP259187.RALLVhSuDRESoH9-mhe2IDWmV-moFXlqpe5LL_RKv2jc4130_assertion evidence source_evidence_literature NP259187.RALLVhSuDRESoH9-mhe2IDWmV-moFXlqpe5LL_RKv2jc4130_provenance.
- NP259187.RALLVhSuDRESoH9-mhe2IDWmV-moFXlqpe5LL_RKv2jc4130_assertion description "[Our genome-wide association study (GWAS) has identified common variants within FLJ22536, BARD1, and LMO1 as significantly associated with neuroblastoma and more robustly associated with high-risk disease.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP259187.RALLVhSuDRESoH9-mhe2IDWmV-moFXlqpe5LL_RKv2jc4130_provenance.