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- source_evidence_literature type ECO_0000212 NP728563.RAh2qQUwMboDbd21A2erJJVlIltScrdixC5M-Jm4eg_FY130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP728563.RAh2qQUwMboDbd21A2erJJVlIltScrdixC5M-Jm4eg_FY130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP728563.RAh2qQUwMboDbd21A2erJJVlIltScrdixC5M-Jm4eg_FY130_provenance.
- NP728563.RAh2qQUwMboDbd21A2erJJVlIltScrdixC5M-Jm4eg_FY130_assertion description "[A systematic RNA interference screen to interrogate the function of each gene in the common deleted region (CDR) for the 5q- syndrome identified RPS14 as a critical haploinsufficiency disease gene for the erythroid failure, which is a characteristic of this syndrome.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP728563.RAh2qQUwMboDbd21A2erJJVlIltScrdixC5M-Jm4eg_FY130_provenance.
- NP728563.RAh2qQUwMboDbd21A2erJJVlIltScrdixC5M-Jm4eg_FY130_assertion evidence source_evidence_literature NP728563.RAh2qQUwMboDbd21A2erJJVlIltScrdixC5M-Jm4eg_FY130_provenance.
- NP728563.RAh2qQUwMboDbd21A2erJJVlIltScrdixC5M-Jm4eg_FY130_assertion SIO_000772 19322210 NP728563.RAh2qQUwMboDbd21A2erJJVlIltScrdixC5M-Jm4eg_FY130_provenance.
- NP728563.RAh2qQUwMboDbd21A2erJJVlIltScrdixC5M-Jm4eg_FY130_assertion wasDerivedFrom befree-2016 NP728563.RAh2qQUwMboDbd21A2erJJVlIltScrdixC5M-Jm4eg_FY130_provenance.
- NP728563.RAh2qQUwMboDbd21A2erJJVlIltScrdixC5M-Jm4eg_FY130_assertion wasGeneratedBy ECO_0000203 NP728563.RAh2qQUwMboDbd21A2erJJVlIltScrdixC5M-Jm4eg_FY130_provenance.
- befree-2016 importedOn "2016-02-19" NP728563.RAh2qQUwMboDbd21A2erJJVlIltScrdixC5M-Jm4eg_FY130_provenance.