Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP1397585.RAjU9UltlzhQgVP6Y4SNt67BE4obTZwPzf7wsTwnnlHAI130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP1397585.RAjU9UltlzhQgVP6Y4SNt67BE4obTZwPzf7wsTwnnlHAI130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP1397585.RAjU9UltlzhQgVP6Y4SNt67BE4obTZwPzf7wsTwnnlHAI130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP1397585.RAjU9UltlzhQgVP6Y4SNt67BE4obTZwPzf7wsTwnnlHAI130_provenance.
- NP1397585.RAjU9UltlzhQgVP6Y4SNt67BE4obTZwPzf7wsTwnnlHAI130_assertion description "[Contribution of two missense mutations (G71R and Y486D) of the bilirubin UDP glycosyltransferase (UGT1A1) gene to phenotypes of Gilbert's syndrome and Crigler-Najjar syndrome type II.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1397585.RAjU9UltlzhQgVP6Y4SNt67BE4obTZwPzf7wsTwnnlHAI130_provenance.
- NP1397585.RAjU9UltlzhQgVP6Y4SNt67BE4obTZwPzf7wsTwnnlHAI130_assertion evidence source_evidence_literature NP1397585.RAjU9UltlzhQgVP6Y4SNt67BE4obTZwPzf7wsTwnnlHAI130_provenance.
- NP1397585.RAjU9UltlzhQgVP6Y4SNt67BE4obTZwPzf7wsTwnnlHAI130_assertion SIO_000772 9630669 NP1397585.RAjU9UltlzhQgVP6Y4SNt67BE4obTZwPzf7wsTwnnlHAI130_provenance.
- NP1397585.RAjU9UltlzhQgVP6Y4SNt67BE4obTZwPzf7wsTwnnlHAI130_assertion wasDerivedFrom befree-2016 NP1397585.RAjU9UltlzhQgVP6Y4SNt67BE4obTZwPzf7wsTwnnlHAI130_provenance.
- NP1397585.RAjU9UltlzhQgVP6Y4SNt67BE4obTZwPzf7wsTwnnlHAI130_assertion wasGeneratedBy ECO_0000203 NP1397585.RAjU9UltlzhQgVP6Y4SNt67BE4obTZwPzf7wsTwnnlHAI130_provenance.
- befree-2016 importedOn "2016-02-19" NP1397585.RAjU9UltlzhQgVP6Y4SNt67BE4obTZwPzf7wsTwnnlHAI130_provenance.