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- source_evidence_literature type ECO_0000212 NP440057.RAWYDhyao3Il47-Hu_ecelunRFzHxtO7LMHcaVtwcqbXA130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP440057.RAWYDhyao3Il47-Hu_ecelunRFzHxtO7LMHcaVtwcqbXA130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP440057.RAWYDhyao3Il47-Hu_ecelunRFzHxtO7LMHcaVtwcqbXA130_provenance.
- NP440057.RAWYDhyao3Il47-Hu_ecelunRFzHxtO7LMHcaVtwcqbXA130_assertion wasGeneratedBy ECO_0000203 NP440057.RAWYDhyao3Il47-Hu_ecelunRFzHxtO7LMHcaVtwcqbXA130_provenance.
- NP440057.RAWYDhyao3Il47-Hu_ecelunRFzHxtO7LMHcaVtwcqbXA130_assertion wasDerivedFrom befree-20140225 NP440057.RAWYDhyao3Il47-Hu_ecelunRFzHxtO7LMHcaVtwcqbXA130_provenance.
- NP440057.RAWYDhyao3Il47-Hu_ecelunRFzHxtO7LMHcaVtwcqbXA130_assertion SIO_000772 10359058 NP440057.RAWYDhyao3Il47-Hu_ecelunRFzHxtO7LMHcaVtwcqbXA130_provenance.
- NP440057.RAWYDhyao3Il47-Hu_ecelunRFzHxtO7LMHcaVtwcqbXA130_assertion evidence source_evidence_literature NP440057.RAWYDhyao3Il47-Hu_ecelunRFzHxtO7LMHcaVtwcqbXA130_provenance.
- NP440057.RAWYDhyao3Il47-Hu_ecelunRFzHxtO7LMHcaVtwcqbXA130_assertion description "[These findings imply a contribution of the UGT1A polymorphism associated to Gilbert's syndrome to development of the hyperbilirubinemia in G6PD deficient subjects during acute hemolytic anemia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP440057.RAWYDhyao3Il47-Hu_ecelunRFzHxtO7LMHcaVtwcqbXA130_provenance.
- befree-20140225 importedOn "2014-02-25" NP440057.RAWYDhyao3Il47-Hu_ecelunRFzHxtO7LMHcaVtwcqbXA130_provenance.