Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP1343029.RAD3H9q6Ki7knQHSXrfESWqfSUPbokZUj64Fa8vXaH6b0130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP1343029.RAD3H9q6Ki7knQHSXrfESWqfSUPbokZUj64Fa8vXaH6b0130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP1343029.RAD3H9q6Ki7knQHSXrfESWqfSUPbokZUj64Fa8vXaH6b0130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP1343029.RAD3H9q6Ki7knQHSXrfESWqfSUPbokZUj64Fa8vXaH6b0130_provenance.
- NP1343029.RAD3H9q6Ki7knQHSXrfESWqfSUPbokZUj64Fa8vXaH6b0130_assertion description "[More than two hundred characterized 21-hydroxylase deficiency alleles appear to result exclusively from sequence exchanges involving the 21-hydroxylase gene (CYP21B) and a closely related pseudogene (CYP21A).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1343029.RAD3H9q6Ki7knQHSXrfESWqfSUPbokZUj64Fa8vXaH6b0130_provenance.
- NP1343029.RAD3H9q6Ki7knQHSXrfESWqfSUPbokZUj64Fa8vXaH6b0130_assertion evidence source_evidence_literature NP1343029.RAD3H9q6Ki7knQHSXrfESWqfSUPbokZUj64Fa8vXaH6b0130_provenance.
- NP1343029.RAD3H9q6Ki7knQHSXrfESWqfSUPbokZUj64Fa8vXaH6b0130_assertion SIO_000772 8485582 NP1343029.RAD3H9q6Ki7knQHSXrfESWqfSUPbokZUj64Fa8vXaH6b0130_provenance.
- NP1343029.RAD3H9q6Ki7knQHSXrfESWqfSUPbokZUj64Fa8vXaH6b0130_assertion wasDerivedFrom befree-2016 NP1343029.RAD3H9q6Ki7knQHSXrfESWqfSUPbokZUj64Fa8vXaH6b0130_provenance.
- NP1343029.RAD3H9q6Ki7knQHSXrfESWqfSUPbokZUj64Fa8vXaH6b0130_assertion wasGeneratedBy ECO_0000203 NP1343029.RAD3H9q6Ki7knQHSXrfESWqfSUPbokZUj64Fa8vXaH6b0130_provenance.
- befree-2016 importedOn "2016-02-19" NP1343029.RAD3H9q6Ki7knQHSXrfESWqfSUPbokZUj64Fa8vXaH6b0130_provenance.