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- source_evidence_literature type ECO_0000212 NP770715.RAqcKHGaaOTcJfCCTrPNhbS9pXVsdo_pkD8K3bsxmt_Q4130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP770715.RAqcKHGaaOTcJfCCTrPNhbS9pXVsdo_pkD8K3bsxmt_Q4130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP770715.RAqcKHGaaOTcJfCCTrPNhbS9pXVsdo_pkD8K3bsxmt_Q4130_provenance.
- NP770715.RAqcKHGaaOTcJfCCTrPNhbS9pXVsdo_pkD8K3bsxmt_Q4130_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." NP770715.RAqcKHGaaOTcJfCCTrPNhbS9pXVsdo_pkD8K3bsxmt_Q4130_provenance.
- NP770715.RAqcKHGaaOTcJfCCTrPNhbS9pXVsdo_pkD8K3bsxmt_Q4130_assertion evidence source_evidence_literature NP770715.RAqcKHGaaOTcJfCCTrPNhbS9pXVsdo_pkD8K3bsxmt_Q4130_provenance.
- NP770715.RAqcKHGaaOTcJfCCTrPNhbS9pXVsdo_pkD8K3bsxmt_Q4130_assertion SIO_000772 19845429 NP770715.RAqcKHGaaOTcJfCCTrPNhbS9pXVsdo_pkD8K3bsxmt_Q4130_provenance.
- NP770715.RAqcKHGaaOTcJfCCTrPNhbS9pXVsdo_pkD8K3bsxmt_Q4130_assertion wasDerivedFrom befree-2016 NP770715.RAqcKHGaaOTcJfCCTrPNhbS9pXVsdo_pkD8K3bsxmt_Q4130_provenance.
- NP770715.RAqcKHGaaOTcJfCCTrPNhbS9pXVsdo_pkD8K3bsxmt_Q4130_assertion wasGeneratedBy ECO_0000203 NP770715.RAqcKHGaaOTcJfCCTrPNhbS9pXVsdo_pkD8K3bsxmt_Q4130_provenance.
- befree-2016 importedOn "2016-02-19" NP770715.RAqcKHGaaOTcJfCCTrPNhbS9pXVsdo_pkD8K3bsxmt_Q4130_provenance.