Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP413416.RAjmVX53ow0rl63jqmyLJL8Qwm2O76cYPNsctibTnKdKM130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP413416.RAjmVX53ow0rl63jqmyLJL8Qwm2O76cYPNsctibTnKdKM130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP413416.RAjmVX53ow0rl63jqmyLJL8Qwm2O76cYPNsctibTnKdKM130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP413416.RAjmVX53ow0rl63jqmyLJL8Qwm2O76cYPNsctibTnKdKM130_provenance.
- NP413416.RAjmVX53ow0rl63jqmyLJL8Qwm2O76cYPNsctibTnKdKM130_assertion description "[The frequency of NR5A1 mutations in otherwise unexplained 46,XY DSD with underandrogenization and partial testicular dysgenesis has been estimated to be about 15%.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP413416.RAjmVX53ow0rl63jqmyLJL8Qwm2O76cYPNsctibTnKdKM130_provenance.
- NP413416.RAjmVX53ow0rl63jqmyLJL8Qwm2O76cYPNsctibTnKdKM130_assertion evidence source_evidence_literature NP413416.RAjmVX53ow0rl63jqmyLJL8Qwm2O76cYPNsctibTnKdKM130_provenance.
- NP413416.RAjmVX53ow0rl63jqmyLJL8Qwm2O76cYPNsctibTnKdKM130_assertion SIO_000772 20595937 NP413416.RAjmVX53ow0rl63jqmyLJL8Qwm2O76cYPNsctibTnKdKM130_provenance.
- NP413416.RAjmVX53ow0rl63jqmyLJL8Qwm2O76cYPNsctibTnKdKM130_assertion wasDerivedFrom befree-20150227 NP413416.RAjmVX53ow0rl63jqmyLJL8Qwm2O76cYPNsctibTnKdKM130_provenance.
- NP413416.RAjmVX53ow0rl63jqmyLJL8Qwm2O76cYPNsctibTnKdKM130_assertion wasGeneratedBy ECO_0000203 NP413416.RAjmVX53ow0rl63jqmyLJL8Qwm2O76cYPNsctibTnKdKM130_provenance.
- befree-20150227 importedOn "2015-02-27" NP413416.RAjmVX53ow0rl63jqmyLJL8Qwm2O76cYPNsctibTnKdKM130_provenance.