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- source_evidence_literature type ECO_0000212 NP512723.RAh8jDBe4S3TZWDdI-F-ArCetNU5hlrnPw9bXKTfBNurM130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP512723.RAh8jDBe4S3TZWDdI-F-ArCetNU5hlrnPw9bXKTfBNurM130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP512723.RAh8jDBe4S3TZWDdI-F-ArCetNU5hlrnPw9bXKTfBNurM130_provenance.
- NP512723.RAh8jDBe4S3TZWDdI-F-ArCetNU5hlrnPw9bXKTfBNurM130_assertion description "[Clinical contributors to hyperbilirubinemia were identified more frequently for case subjects but individually G6PD, UGT1A1, and SLCO1B1 variants were not.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP512723.RAh8jDBe4S3TZWDdI-F-ArCetNU5hlrnPw9bXKTfBNurM130_provenance.
- NP512723.RAh8jDBe4S3TZWDdI-F-ArCetNU5hlrnPw9bXKTfBNurM130_assertion evidence source_evidence_literature NP512723.RAh8jDBe4S3TZWDdI-F-ArCetNU5hlrnPw9bXKTfBNurM130_provenance.
- NP512723.RAh8jDBe4S3TZWDdI-F-ArCetNU5hlrnPw9bXKTfBNurM130_assertion SIO_000772 19858149 NP512723.RAh8jDBe4S3TZWDdI-F-ArCetNU5hlrnPw9bXKTfBNurM130_provenance.
- NP512723.RAh8jDBe4S3TZWDdI-F-ArCetNU5hlrnPw9bXKTfBNurM130_assertion wasDerivedFrom befree-20140225 NP512723.RAh8jDBe4S3TZWDdI-F-ArCetNU5hlrnPw9bXKTfBNurM130_provenance.
- NP512723.RAh8jDBe4S3TZWDdI-F-ArCetNU5hlrnPw9bXKTfBNurM130_assertion wasGeneratedBy ECO_0000203 NP512723.RAh8jDBe4S3TZWDdI-F-ArCetNU5hlrnPw9bXKTfBNurM130_provenance.
- befree-20140225 importedOn "2014-02-25" NP512723.RAh8jDBe4S3TZWDdI-F-ArCetNU5hlrnPw9bXKTfBNurM130_provenance.