Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP800089.RAoBjYAmeAcMA8PcZUoJT9Mza1Wc3dt8c0r0wY0gxdXCg130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP800089.RAoBjYAmeAcMA8PcZUoJT9Mza1Wc3dt8c0r0wY0gxdXCg130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP800089.RAoBjYAmeAcMA8PcZUoJT9Mza1Wc3dt8c0r0wY0gxdXCg130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP800089.RAoBjYAmeAcMA8PcZUoJT9Mza1Wc3dt8c0r0wY0gxdXCg130_provenance.
- NP800089.RAoBjYAmeAcMA8PcZUoJT9Mza1Wc3dt8c0r0wY0gxdXCg130_assertion description "[The common P450 oxidoreductase variant A503V is not a modifier gene for 21-hydroxylase deficiency.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP800089.RAoBjYAmeAcMA8PcZUoJT9Mza1Wc3dt8c0r0wY0gxdXCg130_provenance.
- NP800089.RAoBjYAmeAcMA8PcZUoJT9Mza1Wc3dt8c0r0wY0gxdXCg130_assertion evidence source_evidence_literature NP800089.RAoBjYAmeAcMA8PcZUoJT9Mza1Wc3dt8c0r0wY0gxdXCg130_provenance.
- NP800089.RAoBjYAmeAcMA8PcZUoJT9Mza1Wc3dt8c0r0wY0gxdXCg130_assertion SIO_000772 18397975 NP800089.RAoBjYAmeAcMA8PcZUoJT9Mza1Wc3dt8c0r0wY0gxdXCg130_provenance.
- NP800089.RAoBjYAmeAcMA8PcZUoJT9Mza1Wc3dt8c0r0wY0gxdXCg130_assertion wasDerivedFrom befree-20150227 NP800089.RAoBjYAmeAcMA8PcZUoJT9Mza1Wc3dt8c0r0wY0gxdXCg130_provenance.
- NP800089.RAoBjYAmeAcMA8PcZUoJT9Mza1Wc3dt8c0r0wY0gxdXCg130_assertion wasGeneratedBy ECO_0000203 NP800089.RAoBjYAmeAcMA8PcZUoJT9Mza1Wc3dt8c0r0wY0gxdXCg130_provenance.
- befree-20150227 importedOn "2015-02-27" NP800089.RAoBjYAmeAcMA8PcZUoJT9Mza1Wc3dt8c0r0wY0gxdXCg130_provenance.