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- source_evidence_literature type ECO_0000212 NP766299.RADF7wZyUdQXYGdZEToYHRe80-7pwEDDIyCy8ZJ6wmwmA130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP766299.RADF7wZyUdQXYGdZEToYHRe80-7pwEDDIyCy8ZJ6wmwmA130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP766299.RADF7wZyUdQXYGdZEToYHRe80-7pwEDDIyCy8ZJ6wmwmA130_provenance.
- befree-20150227 importedOn "2015-02-27" NP766299.RADF7wZyUdQXYGdZEToYHRe80-7pwEDDIyCy8ZJ6wmwmA130_provenance.
- NP766299.RADF7wZyUdQXYGdZEToYHRe80-7pwEDDIyCy8ZJ6wmwmA130_assertion wasGeneratedBy ECO_0000203 NP766299.RADF7wZyUdQXYGdZEToYHRe80-7pwEDDIyCy8ZJ6wmwmA130_provenance.
- NP766299.RADF7wZyUdQXYGdZEToYHRe80-7pwEDDIyCy8ZJ6wmwmA130_assertion wasDerivedFrom befree-20150227 NP766299.RADF7wZyUdQXYGdZEToYHRe80-7pwEDDIyCy8ZJ6wmwmA130_provenance.
- NP766299.RADF7wZyUdQXYGdZEToYHRe80-7pwEDDIyCy8ZJ6wmwmA130_assertion SIO_000772 16623861 NP766299.RADF7wZyUdQXYGdZEToYHRe80-7pwEDDIyCy8ZJ6wmwmA130_provenance.
- NP766299.RADF7wZyUdQXYGdZEToYHRe80-7pwEDDIyCy8ZJ6wmwmA130_assertion evidence source_evidence_literature NP766299.RADF7wZyUdQXYGdZEToYHRe80-7pwEDDIyCy8ZJ6wmwmA130_provenance.
- NP766299.RADF7wZyUdQXYGdZEToYHRe80-7pwEDDIyCy8ZJ6wmwmA130_assertion description "[Variations in B-UGT gene (UGT-1A1) have been related to disorders characterised by hyperbilirubinaemia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP766299.RADF7wZyUdQXYGdZEToYHRe80-7pwEDDIyCy8ZJ6wmwmA130_provenance.