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- source_evidence_literature type ECO_0000212 NP1170527.RA37X2AxUlOg-GIo5TnR_YSrs9mhWq5VIjT8cGEyl-kZA130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP1170527.RA37X2AxUlOg-GIo5TnR_YSrs9mhWq5VIjT8cGEyl-kZA130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP1170527.RA37X2AxUlOg-GIo5TnR_YSrs9mhWq5VIjT8cGEyl-kZA130_provenance.
- NP1170527.RA37X2AxUlOg-GIo5TnR_YSrs9mhWq5VIjT8cGEyl-kZA130_assertion description "[These findings illustrate the value of SNP arrays for the detection of novel recurrent genomic alterations that may contribute to CLL/SLL onset or progression.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1170527.RA37X2AxUlOg-GIo5TnR_YSrs9mhWq5VIjT8cGEyl-kZA130_provenance.
- NP1170527.RA37X2AxUlOg-GIo5TnR_YSrs9mhWq5VIjT8cGEyl-kZA130_assertion evidence source_evidence_literature NP1170527.RA37X2AxUlOg-GIo5TnR_YSrs9mhWq5VIjT8cGEyl-kZA130_provenance.
- NP1170527.RA37X2AxUlOg-GIo5TnR_YSrs9mhWq5VIjT8cGEyl-kZA130_assertion SIO_000772 24704113 NP1170527.RA37X2AxUlOg-GIo5TnR_YSrs9mhWq5VIjT8cGEyl-kZA130_provenance.
- NP1170527.RA37X2AxUlOg-GIo5TnR_YSrs9mhWq5VIjT8cGEyl-kZA130_assertion wasDerivedFrom befree-2016 NP1170527.RA37X2AxUlOg-GIo5TnR_YSrs9mhWq5VIjT8cGEyl-kZA130_provenance.
- NP1170527.RA37X2AxUlOg-GIo5TnR_YSrs9mhWq5VIjT8cGEyl-kZA130_assertion wasGeneratedBy ECO_0000203 NP1170527.RA37X2AxUlOg-GIo5TnR_YSrs9mhWq5VIjT8cGEyl-kZA130_provenance.
- befree-2016 importedOn "2016-02-19" NP1170527.RA37X2AxUlOg-GIo5TnR_YSrs9mhWq5VIjT8cGEyl-kZA130_provenance.