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- source_evidence_literature type ECO_0000212 NP765926.RApbMUwZUJVlNTY-OeZJJ_yIkagyh8SYanS1w076RpUSo130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP765926.RApbMUwZUJVlNTY-OeZJJ_yIkagyh8SYanS1w076RpUSo130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP765926.RApbMUwZUJVlNTY-OeZJJ_yIkagyh8SYanS1w076RpUSo130_provenance.
- NP765926.RApbMUwZUJVlNTY-OeZJJ_yIkagyh8SYanS1w076RpUSo130_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." NP765926.RApbMUwZUJVlNTY-OeZJJ_yIkagyh8SYanS1w076RpUSo130_provenance.
- NP765926.RApbMUwZUJVlNTY-OeZJJ_yIkagyh8SYanS1w076RpUSo130_assertion evidence source_evidence_literature NP765926.RApbMUwZUJVlNTY-OeZJJ_yIkagyh8SYanS1w076RpUSo130_provenance.
- NP765926.RApbMUwZUJVlNTY-OeZJJ_yIkagyh8SYanS1w076RpUSo130_assertion SIO_000772 19845429 NP765926.RApbMUwZUJVlNTY-OeZJJ_yIkagyh8SYanS1w076RpUSo130_provenance.
- NP765926.RApbMUwZUJVlNTY-OeZJJ_yIkagyh8SYanS1w076RpUSo130_assertion wasDerivedFrom befree-20150227 NP765926.RApbMUwZUJVlNTY-OeZJJ_yIkagyh8SYanS1w076RpUSo130_provenance.
- NP765926.RApbMUwZUJVlNTY-OeZJJ_yIkagyh8SYanS1w076RpUSo130_assertion wasGeneratedBy ECO_0000203 NP765926.RApbMUwZUJVlNTY-OeZJJ_yIkagyh8SYanS1w076RpUSo130_provenance.
- befree-20150227 importedOn "2015-02-27" NP765926.RApbMUwZUJVlNTY-OeZJJ_yIkagyh8SYanS1w076RpUSo130_provenance.