Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP20826.RAbE_joUty0Fxp2xLBqwFBeKwj8ToN2lRJ1gphn1wKII8130_provenance>. }
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- source_evidence_curated type ECO_0000205 NP20826.RAbE_joUty0Fxp2xLBqwFBeKwj8ToN2lRJ1gphn1wKII8130_provenance.
- source_evidence_curated label "DisGeNET evidence - CURATED" NP20826.RAbE_joUty0Fxp2xLBqwFBeKwj8ToN2lRJ1gphn1wKII8130_provenance.
- source_evidence_curated comment "Gene-disease associations manually curated." NP20826.RAbE_joUty0Fxp2xLBqwFBeKwj8ToN2lRJ1gphn1wKII8130_provenance.
- NP20826.RAbE_joUty0Fxp2xLBqwFBeKwj8ToN2lRJ1gphn1wKII8130_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." NP20826.RAbE_joUty0Fxp2xLBqwFBeKwj8ToN2lRJ1gphn1wKII8130_provenance.
- NP20826.RAbE_joUty0Fxp2xLBqwFBeKwj8ToN2lRJ1gphn1wKII8130_assertion evidence source_evidence_curated NP20826.RAbE_joUty0Fxp2xLBqwFBeKwj8ToN2lRJ1gphn1wKII8130_provenance.
- NP20826.RAbE_joUty0Fxp2xLBqwFBeKwj8ToN2lRJ1gphn1wKII8130_assertion SIO_000772 18006695 NP20826.RAbE_joUty0Fxp2xLBqwFBeKwj8ToN2lRJ1gphn1wKII8130_provenance.
- NP20826.RAbE_joUty0Fxp2xLBqwFBeKwj8ToN2lRJ1gphn1wKII8130_assertion wasDerivedFrom ctd_human-2016 NP20826.RAbE_joUty0Fxp2xLBqwFBeKwj8ToN2lRJ1gphn1wKII8130_provenance.
- NP20826.RAbE_joUty0Fxp2xLBqwFBeKwj8ToN2lRJ1gphn1wKII8130_assertion wasGeneratedBy ECO_0000218 NP20826.RAbE_joUty0Fxp2xLBqwFBeKwj8ToN2lRJ1gphn1wKII8130_provenance.
- ctd_human-2016 importedOn "2016-01-25" NP20826.RAbE_joUty0Fxp2xLBqwFBeKwj8ToN2lRJ1gphn1wKII8130_provenance.