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- NP475376.RAa7AT60nlB63dVVYSHTMaOlDYNE4ytou83S-wrVGTNuI130_assertion type Assertion NP475376.RAa7AT60nlB63dVVYSHTMaOlDYNE4ytou83S-wrVGTNuI130_head.
- NP475376.RAa7AT60nlB63dVVYSHTMaOlDYNE4ytou83S-wrVGTNuI130_assertion description "[In addition, the haplotype of CYP21 with chimera CYP21P/CYP21 causes 21-hydroxylase deficiency in congenital adrenal hyperplasia (CAH), while chimera TNXA/TNXB is associated with Ehlers-Danols syndrome as well as CAH.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP475376.RAa7AT60nlB63dVVYSHTMaOlDYNE4ytou83S-wrVGTNuI130_provenance.
- NP475376.RAa7AT60nlB63dVVYSHTMaOlDYNE4ytou83S-wrVGTNuI130_assertion evidence source_evidence_literature NP475376.RAa7AT60nlB63dVVYSHTMaOlDYNE4ytou83S-wrVGTNuI130_provenance.
- NP475376.RAa7AT60nlB63dVVYSHTMaOlDYNE4ytou83S-wrVGTNuI130_assertion SIO_000772 15639189 NP475376.RAa7AT60nlB63dVVYSHTMaOlDYNE4ytou83S-wrVGTNuI130_provenance.
- NP475376.RAa7AT60nlB63dVVYSHTMaOlDYNE4ytou83S-wrVGTNuI130_assertion wasDerivedFrom befree-2016 NP475376.RAa7AT60nlB63dVVYSHTMaOlDYNE4ytou83S-wrVGTNuI130_provenance.
- NP475376.RAa7AT60nlB63dVVYSHTMaOlDYNE4ytou83S-wrVGTNuI130_assertion wasGeneratedBy ECO_0000203 NP475376.RAa7AT60nlB63dVVYSHTMaOlDYNE4ytou83S-wrVGTNuI130_provenance.