Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP924379.RAMBPcRCtzJ6vryhJhmpn7d7gT5CMhSnH9UyXj5YKj-n0130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP924379.RAMBPcRCtzJ6vryhJhmpn7d7gT5CMhSnH9UyXj5YKj-n0130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP924379.RAMBPcRCtzJ6vryhJhmpn7d7gT5CMhSnH9UyXj5YKj-n0130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP924379.RAMBPcRCtzJ6vryhJhmpn7d7gT5CMhSnH9UyXj5YKj-n0130_provenance.
- NP924379.RAMBPcRCtzJ6vryhJhmpn7d7gT5CMhSnH9UyXj5YKj-n0130_assertion description "[Now, examination of the UGT1 gene structure in hyperbilirubinemic patients has revealed more than 100 different genetic defects in Crigler-Najjar syndromes and one genetic alternation that accounts for the majority of Gilbert's syndrome cases.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP924379.RAMBPcRCtzJ6vryhJhmpn7d7gT5CMhSnH9UyXj5YKj-n0130_provenance.
- NP924379.RAMBPcRCtzJ6vryhJhmpn7d7gT5CMhSnH9UyXj5YKj-n0130_assertion evidence source_evidence_literature NP924379.RAMBPcRCtzJ6vryhJhmpn7d7gT5CMhSnH9UyXj5YKj-n0130_provenance.
- NP924379.RAMBPcRCtzJ6vryhJhmpn7d7gT5CMhSnH9UyXj5YKj-n0130_assertion SIO_000772 19845429 NP924379.RAMBPcRCtzJ6vryhJhmpn7d7gT5CMhSnH9UyXj5YKj-n0130_provenance.
- NP924379.RAMBPcRCtzJ6vryhJhmpn7d7gT5CMhSnH9UyXj5YKj-n0130_assertion wasDerivedFrom befree-20150227 NP924379.RAMBPcRCtzJ6vryhJhmpn7d7gT5CMhSnH9UyXj5YKj-n0130_provenance.
- NP924379.RAMBPcRCtzJ6vryhJhmpn7d7gT5CMhSnH9UyXj5YKj-n0130_assertion wasGeneratedBy ECO_0000203 NP924379.RAMBPcRCtzJ6vryhJhmpn7d7gT5CMhSnH9UyXj5YKj-n0130_provenance.
- befree-20150227 importedOn "2015-02-27" NP924379.RAMBPcRCtzJ6vryhJhmpn7d7gT5CMhSnH9UyXj5YKj-n0130_provenance.