Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP20830.RADwERnCutJsIxu34qbmM0Y4w5A3dP343d-f6Yy3WH-N0130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_curated type ECO_0000205 NP20830.RADwERnCutJsIxu34qbmM0Y4w5A3dP343d-f6Yy3WH-N0130_provenance.
- source_evidence_curated label "DisGeNET evidence - CURATED" NP20830.RADwERnCutJsIxu34qbmM0Y4w5A3dP343d-f6Yy3WH-N0130_provenance.
- source_evidence_curated comment "Gene-disease associations manually curated." NP20830.RADwERnCutJsIxu34qbmM0Y4w5A3dP343d-f6Yy3WH-N0130_provenance.
- NP20830.RADwERnCutJsIxu34qbmM0Y4w5A3dP343d-f6Yy3WH-N0130_assertion description "[Scan of 977 nonsynonymous SNPs in CLL4 trial patients for the identification of genetic variants influencing prognosis.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP20830.RADwERnCutJsIxu34qbmM0Y4w5A3dP343d-f6Yy3WH-N0130_provenance.
- NP20830.RADwERnCutJsIxu34qbmM0Y4w5A3dP343d-f6Yy3WH-N0130_assertion evidence source_evidence_curated NP20830.RADwERnCutJsIxu34qbmM0Y4w5A3dP343d-f6Yy3WH-N0130_provenance.
- NP20830.RADwERnCutJsIxu34qbmM0Y4w5A3dP343d-f6Yy3WH-N0130_assertion SIO_000772 18006695 NP20830.RADwERnCutJsIxu34qbmM0Y4w5A3dP343d-f6Yy3WH-N0130_provenance.
- NP20830.RADwERnCutJsIxu34qbmM0Y4w5A3dP343d-f6Yy3WH-N0130_assertion wasDerivedFrom ctd_human-2016 NP20830.RADwERnCutJsIxu34qbmM0Y4w5A3dP343d-f6Yy3WH-N0130_provenance.
- NP20830.RADwERnCutJsIxu34qbmM0Y4w5A3dP343d-f6Yy3WH-N0130_assertion wasGeneratedBy ECO_0000218 NP20830.RADwERnCutJsIxu34qbmM0Y4w5A3dP343d-f6Yy3WH-N0130_provenance.
- ctd_human-2016 importedOn "2016-01-25" NP20830.RADwERnCutJsIxu34qbmM0Y4w5A3dP343d-f6Yy3WH-N0130_provenance.