Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP308786.RAh5M6RimwdP4jA_74HTvpQ_UUOEI79U9DScw-n4ofvBM130_assertion> ?p ?o ?g. }
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- NP308786.RAh5M6RimwdP4jA_74HTvpQ_UUOEI79U9DScw-n4ofvBM130_assertion type Assertion NP308786.RAh5M6RimwdP4jA_74HTvpQ_UUOEI79U9DScw-n4ofvBM130_head.
- NP308786.RAh5M6RimwdP4jA_74HTvpQ_UUOEI79U9DScw-n4ofvBM130_assertion description "[Our results confirm the significant contribution of ARX mutations in the etiology of MR, especially in this group of patients selected for XLMR (3%).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP308786.RAh5M6RimwdP4jA_74HTvpQ_UUOEI79U9DScw-n4ofvBM130_provenance.
- NP308786.RAh5M6RimwdP4jA_74HTvpQ_UUOEI79U9DScw-n4ofvBM130_assertion evidence source_evidence_literature NP308786.RAh5M6RimwdP4jA_74HTvpQ_UUOEI79U9DScw-n4ofvBM130_provenance.
- NP308786.RAh5M6RimwdP4jA_74HTvpQ_UUOEI79U9DScw-n4ofvBM130_assertion SIO_000772 16523516 NP308786.RAh5M6RimwdP4jA_74HTvpQ_UUOEI79U9DScw-n4ofvBM130_provenance.
- NP308786.RAh5M6RimwdP4jA_74HTvpQ_UUOEI79U9DScw-n4ofvBM130_assertion wasDerivedFrom befree-20140225 NP308786.RAh5M6RimwdP4jA_74HTvpQ_UUOEI79U9DScw-n4ofvBM130_provenance.
- NP308786.RAh5M6RimwdP4jA_74HTvpQ_UUOEI79U9DScw-n4ofvBM130_assertion wasGeneratedBy ECO_0000203 NP308786.RAh5M6RimwdP4jA_74HTvpQ_UUOEI79U9DScw-n4ofvBM130_provenance.