Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP717684.RAXHUGy24GTZglYTRm10Pq0QLr_b_npSBjwhUhGg-sdOs130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP717684.RAXHUGy24GTZglYTRm10Pq0QLr_b_npSBjwhUhGg-sdOs130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP717684.RAXHUGy24GTZglYTRm10Pq0QLr_b_npSBjwhUhGg-sdOs130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP717684.RAXHUGy24GTZglYTRm10Pq0QLr_b_npSBjwhUhGg-sdOs130_provenance.
- NP717684.RAXHUGy24GTZglYTRm10Pq0QLr_b_npSBjwhUhGg-sdOs130_assertion description "[Crigler-Najjar syndrome (CNS), caused by deficiency of bilirubin uridine diphosphate glucuronosyltransferase (UGT) 1A1, is a rare and autosomal recessive inherited disorder characterized by severe unconjugated nonhemolytic hyperbilirubinemia since birth.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP717684.RAXHUGy24GTZglYTRm10Pq0QLr_b_npSBjwhUhGg-sdOs130_provenance.
- NP717684.RAXHUGy24GTZglYTRm10Pq0QLr_b_npSBjwhUhGg-sdOs130_assertion evidence source_evidence_literature NP717684.RAXHUGy24GTZglYTRm10Pq0QLr_b_npSBjwhUhGg-sdOs130_provenance.
- NP717684.RAXHUGy24GTZglYTRm10Pq0QLr_b_npSBjwhUhGg-sdOs130_assertion SIO_000772 24341141 NP717684.RAXHUGy24GTZglYTRm10Pq0QLr_b_npSBjwhUhGg-sdOs130_provenance.
- NP717684.RAXHUGy24GTZglYTRm10Pq0QLr_b_npSBjwhUhGg-sdOs130_assertion wasDerivedFrom befree-20140225 NP717684.RAXHUGy24GTZglYTRm10Pq0QLr_b_npSBjwhUhGg-sdOs130_provenance.
- NP717684.RAXHUGy24GTZglYTRm10Pq0QLr_b_npSBjwhUhGg-sdOs130_assertion wasGeneratedBy ECO_0000203 NP717684.RAXHUGy24GTZglYTRm10Pq0QLr_b_npSBjwhUhGg-sdOs130_provenance.
- befree-20140225 importedOn "2014-02-25" NP717684.RAXHUGy24GTZglYTRm10Pq0QLr_b_npSBjwhUhGg-sdOs130_provenance.