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- source_evidence_literature type ECO_0000212 NP795057.RAXB6BF0nUWAuAWT_FHRSC9KbWkA7TYW-wVLx8yhubRjA130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP795057.RAXB6BF0nUWAuAWT_FHRSC9KbWkA7TYW-wVLx8yhubRjA130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP795057.RAXB6BF0nUWAuAWT_FHRSC9KbWkA7TYW-wVLx8yhubRjA130_provenance.
- NP795057.RAXB6BF0nUWAuAWT_FHRSC9KbWkA7TYW-wVLx8yhubRjA130_assertion description "[Our study suggests that KIR genotyping of donor and recipient pairs could contribute to the identification of patients at high risk for developing severe complications of haematopoietic SCT and thus may help with the choice of intensity of GVHD prophylaxis.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP795057.RAXB6BF0nUWAuAWT_FHRSC9KbWkA7TYW-wVLx8yhubRjA130_provenance.
- NP795057.RAXB6BF0nUWAuAWT_FHRSC9KbWkA7TYW-wVLx8yhubRjA130_assertion evidence source_evidence_literature NP795057.RAXB6BF0nUWAuAWT_FHRSC9KbWkA7TYW-wVLx8yhubRjA130_provenance.
- NP795057.RAXB6BF0nUWAuAWT_FHRSC9KbWkA7TYW-wVLx8yhubRjA130_assertion SIO_000772 20173792 NP795057.RAXB6BF0nUWAuAWT_FHRSC9KbWkA7TYW-wVLx8yhubRjA130_provenance.
- NP795057.RAXB6BF0nUWAuAWT_FHRSC9KbWkA7TYW-wVLx8yhubRjA130_assertion wasDerivedFrom befree-2016 NP795057.RAXB6BF0nUWAuAWT_FHRSC9KbWkA7TYW-wVLx8yhubRjA130_provenance.
- NP795057.RAXB6BF0nUWAuAWT_FHRSC9KbWkA7TYW-wVLx8yhubRjA130_assertion wasGeneratedBy ECO_0000203 NP795057.RAXB6BF0nUWAuAWT_FHRSC9KbWkA7TYW-wVLx8yhubRjA130_provenance.
- befree-2016 importedOn "2016-02-19" NP795057.RAXB6BF0nUWAuAWT_FHRSC9KbWkA7TYW-wVLx8yhubRjA130_provenance.