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- NP468719.RAcrsayXMWpHJHOKraKXmhQXxqum7EX4QJdvLUsWulCBQ130_assertion type Assertion NP468719.RAcrsayXMWpHJHOKraKXmhQXxqum7EX4QJdvLUsWulCBQ130_head.
- NP468719.RAcrsayXMWpHJHOKraKXmhQXxqum7EX4QJdvLUsWulCBQ130_assertion description "[A new compound heterozygous frameshift mutation in the type II 3 beta-hydroxysteroid dehydrogenase (3 beta-HSD) gene causes salt-wasting 3 beta-HSD deficiency congenital adrenal hyperplasia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP468719.RAcrsayXMWpHJHOKraKXmhQXxqum7EX4QJdvLUsWulCBQ130_provenance.
- NP468719.RAcrsayXMWpHJHOKraKXmhQXxqum7EX4QJdvLUsWulCBQ130_assertion evidence source_evidence_literature NP468719.RAcrsayXMWpHJHOKraKXmhQXxqum7EX4QJdvLUsWulCBQ130_provenance.
- NP468719.RAcrsayXMWpHJHOKraKXmhQXxqum7EX4QJdvLUsWulCBQ130_assertion SIO_000772 8550766 NP468719.RAcrsayXMWpHJHOKraKXmhQXxqum7EX4QJdvLUsWulCBQ130_provenance.
- NP468719.RAcrsayXMWpHJHOKraKXmhQXxqum7EX4QJdvLUsWulCBQ130_assertion wasDerivedFrom befree-20140225 NP468719.RAcrsayXMWpHJHOKraKXmhQXxqum7EX4QJdvLUsWulCBQ130_provenance.
- NP468719.RAcrsayXMWpHJHOKraKXmhQXxqum7EX4QJdvLUsWulCBQ130_assertion wasGeneratedBy ECO_0000203 NP468719.RAcrsayXMWpHJHOKraKXmhQXxqum7EX4QJdvLUsWulCBQ130_provenance.