Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP475371.RA2ppN4UNRQecfg1DzPYE32mLwGiZIto-qXzwNTx4dPHI130_assertion> ?p ?o ?g. }
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- NP475371.RA2ppN4UNRQecfg1DzPYE32mLwGiZIto-qXzwNTx4dPHI130_assertion type Assertion NP475371.RA2ppN4UNRQecfg1DzPYE32mLwGiZIto-qXzwNTx4dPHI130_head.
- NP475371.RA2ppN4UNRQecfg1DzPYE32mLwGiZIto-qXzwNTx4dPHI130_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." NP475371.RA2ppN4UNRQecfg1DzPYE32mLwGiZIto-qXzwNTx4dPHI130_provenance.
- NP475371.RA2ppN4UNRQecfg1DzPYE32mLwGiZIto-qXzwNTx4dPHI130_assertion evidence source_evidence_literature NP475371.RA2ppN4UNRQecfg1DzPYE32mLwGiZIto-qXzwNTx4dPHI130_provenance.
- NP475371.RA2ppN4UNRQecfg1DzPYE32mLwGiZIto-qXzwNTx4dPHI130_assertion SIO_000772 15639189 NP475371.RA2ppN4UNRQecfg1DzPYE32mLwGiZIto-qXzwNTx4dPHI130_provenance.
- NP475371.RA2ppN4UNRQecfg1DzPYE32mLwGiZIto-qXzwNTx4dPHI130_assertion wasDerivedFrom befree-2016 NP475371.RA2ppN4UNRQecfg1DzPYE32mLwGiZIto-qXzwNTx4dPHI130_provenance.
- NP475371.RA2ppN4UNRQecfg1DzPYE32mLwGiZIto-qXzwNTx4dPHI130_assertion wasGeneratedBy ECO_0000203 NP475371.RA2ppN4UNRQecfg1DzPYE32mLwGiZIto-qXzwNTx4dPHI130_provenance.