Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP765946.RAL-QsxymoNviNxGq575HuX6PQ_e4SJMjgY_K-CDwugFQ130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP765946.RAL-QsxymoNviNxGq575HuX6PQ_e4SJMjgY_K-CDwugFQ130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP765946.RAL-QsxymoNviNxGq575HuX6PQ_e4SJMjgY_K-CDwugFQ130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP765946.RAL-QsxymoNviNxGq575HuX6PQ_e4SJMjgY_K-CDwugFQ130_provenance.
- befree-20150227 importedOn "2015-02-27" NP765946.RAL-QsxymoNviNxGq575HuX6PQ_e4SJMjgY_K-CDwugFQ130_provenance.
- NP765946.RAL-QsxymoNviNxGq575HuX6PQ_e4SJMjgY_K-CDwugFQ130_assertion wasGeneratedBy ECO_0000203 NP765946.RAL-QsxymoNviNxGq575HuX6PQ_e4SJMjgY_K-CDwugFQ130_provenance.
- NP765946.RAL-QsxymoNviNxGq575HuX6PQ_e4SJMjgY_K-CDwugFQ130_assertion wasDerivedFrom befree-20150227 NP765946.RAL-QsxymoNviNxGq575HuX6PQ_e4SJMjgY_K-CDwugFQ130_provenance.
- NP765946.RAL-QsxymoNviNxGq575HuX6PQ_e4SJMjgY_K-CDwugFQ130_assertion SIO_000772 8027054 NP765946.RAL-QsxymoNviNxGq575HuX6PQ_e4SJMjgY_K-CDwugFQ130_provenance.
- NP765946.RAL-QsxymoNviNxGq575HuX6PQ_e4SJMjgY_K-CDwugFQ130_assertion evidence source_evidence_literature NP765946.RAL-QsxymoNviNxGq575HuX6PQ_e4SJMjgY_K-CDwugFQ130_provenance.
- NP765946.RAL-QsxymoNviNxGq575HuX6PQ_e4SJMjgY_K-CDwugFQ130_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." NP765946.RAL-QsxymoNviNxGq575HuX6PQ_e4SJMjgY_K-CDwugFQ130_provenance.