Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP761776.RALRjm1WOgqPIrLLC8VTomV1Zuhf3Plf5MS93j28jx-So130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP761776.RALRjm1WOgqPIrLLC8VTomV1Zuhf3Plf5MS93j28jx-So130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP761776.RALRjm1WOgqPIrLLC8VTomV1Zuhf3Plf5MS93j28jx-So130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP761776.RALRjm1WOgqPIrLLC8VTomV1Zuhf3Plf5MS93j28jx-So130_provenance.
- NP761776.RALRjm1WOgqPIrLLC8VTomV1Zuhf3Plf5MS93j28jx-So130_assertion description "[Overall, our study identifies that XPD polymorphisms may be important in the aetiology of NHL although analysis of additional polymorphisms and extended haplotype studies are required to clarify their role.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP761776.RALRjm1WOgqPIrLLC8VTomV1Zuhf3Plf5MS93j28jx-So130_provenance.
- NP761776.RALRjm1WOgqPIrLLC8VTomV1Zuhf3Plf5MS93j28jx-So130_assertion evidence source_evidence_literature NP761776.RALRjm1WOgqPIrLLC8VTomV1Zuhf3Plf5MS93j28jx-So130_provenance.
- NP761776.RALRjm1WOgqPIrLLC8VTomV1Zuhf3Plf5MS93j28jx-So130_assertion SIO_000772 19736055 NP761776.RALRjm1WOgqPIrLLC8VTomV1Zuhf3Plf5MS93j28jx-So130_provenance.
- NP761776.RALRjm1WOgqPIrLLC8VTomV1Zuhf3Plf5MS93j28jx-So130_assertion wasDerivedFrom befree-2016 NP761776.RALRjm1WOgqPIrLLC8VTomV1Zuhf3Plf5MS93j28jx-So130_provenance.
- NP761776.RALRjm1WOgqPIrLLC8VTomV1Zuhf3Plf5MS93j28jx-So130_assertion wasGeneratedBy ECO_0000203 NP761776.RALRjm1WOgqPIrLLC8VTomV1Zuhf3Plf5MS93j28jx-So130_provenance.
- befree-2016 importedOn "2016-02-19" NP761776.RALRjm1WOgqPIrLLC8VTomV1Zuhf3Plf5MS93j28jx-So130_provenance.