Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP671419.RAw3MH5IT3sluja4YtR3Z6KgJptoZuBLSnCHtr0coHmtY130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP671419.RAw3MH5IT3sluja4YtR3Z6KgJptoZuBLSnCHtr0coHmtY130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP671419.RAw3MH5IT3sluja4YtR3Z6KgJptoZuBLSnCHtr0coHmtY130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP671419.RAw3MH5IT3sluja4YtR3Z6KgJptoZuBLSnCHtr0coHmtY130_provenance.
- NP671419.RAw3MH5IT3sluja4YtR3Z6KgJptoZuBLSnCHtr0coHmtY130_assertion description "[Gilbert's Syndrome (GS) and CNS type I both involve abnormalities in bilirubin conjugation secondary to deficiency of bilirubin UGT.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP671419.RAw3MH5IT3sluja4YtR3Z6KgJptoZuBLSnCHtr0coHmtY130_provenance.
- NP671419.RAw3MH5IT3sluja4YtR3Z6KgJptoZuBLSnCHtr0coHmtY130_assertion evidence source_evidence_literature NP671419.RAw3MH5IT3sluja4YtR3Z6KgJptoZuBLSnCHtr0coHmtY130_provenance.
- NP671419.RAw3MH5IT3sluja4YtR3Z6KgJptoZuBLSnCHtr0coHmtY130_assertion SIO_000772 24341141 NP671419.RAw3MH5IT3sluja4YtR3Z6KgJptoZuBLSnCHtr0coHmtY130_provenance.
- NP671419.RAw3MH5IT3sluja4YtR3Z6KgJptoZuBLSnCHtr0coHmtY130_assertion wasDerivedFrom befree-20140225 NP671419.RAw3MH5IT3sluja4YtR3Z6KgJptoZuBLSnCHtr0coHmtY130_provenance.
- NP671419.RAw3MH5IT3sluja4YtR3Z6KgJptoZuBLSnCHtr0coHmtY130_assertion wasGeneratedBy ECO_0000203 NP671419.RAw3MH5IT3sluja4YtR3Z6KgJptoZuBLSnCHtr0coHmtY130_provenance.
- befree-20140225 importedOn "2014-02-25" NP671419.RAw3MH5IT3sluja4YtR3Z6KgJptoZuBLSnCHtr0coHmtY130_provenance.