Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP338987.RAnl8P9WWoq0af0UTP8sntonWaomCpv6vLw4BDJ8lJT5A130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP338987.RAnl8P9WWoq0af0UTP8sntonWaomCpv6vLw4BDJ8lJT5A130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP338987.RAnl8P9WWoq0af0UTP8sntonWaomCpv6vLw4BDJ8lJT5A130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP338987.RAnl8P9WWoq0af0UTP8sntonWaomCpv6vLw4BDJ8lJT5A130_provenance.
- NP338987.RAnl8P9WWoq0af0UTP8sntonWaomCpv6vLw4BDJ8lJT5A130_assertion wasGeneratedBy ECO_0000203 NP338987.RAnl8P9WWoq0af0UTP8sntonWaomCpv6vLw4BDJ8lJT5A130_provenance.
- NP338987.RAnl8P9WWoq0af0UTP8sntonWaomCpv6vLw4BDJ8lJT5A130_assertion wasDerivedFrom befree-20140225 NP338987.RAnl8P9WWoq0af0UTP8sntonWaomCpv6vLw4BDJ8lJT5A130_provenance.
- NP338987.RAnl8P9WWoq0af0UTP8sntonWaomCpv6vLw4BDJ8lJT5A130_assertion SIO_000772 8027054 NP338987.RAnl8P9WWoq0af0UTP8sntonWaomCpv6vLw4BDJ8lJT5A130_provenance.
- NP338987.RAnl8P9WWoq0af0UTP8sntonWaomCpv6vLw4BDJ8lJT5A130_assertion evidence source_evidence_literature NP338987.RAnl8P9WWoq0af0UTP8sntonWaomCpv6vLw4BDJ8lJT5A130_provenance.
- NP338987.RAnl8P9WWoq0af0UTP8sntonWaomCpv6vLw4BDJ8lJT5A130_assertion description "[Crigler-Najjar syndrome type I (CN-I) is caused by an inherited absence of UDP-glucuronosyltransferase activity toward bilirubin (B-UGT), resulting in severe non-hemolytic unconjugated hyperbilirubinemia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP338987.RAnl8P9WWoq0af0UTP8sntonWaomCpv6vLw4BDJ8lJT5A130_provenance.
- befree-20140225 importedOn "2014-02-25" NP338987.RAnl8P9WWoq0af0UTP8sntonWaomCpv6vLw4BDJ8lJT5A130_provenance.