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- NP748914.RAYDl3o4sK2igxPp_wBAz2vry_EHwv4yKQLq8CSZr75JQ130_assertion type Assertion NP748914.RAYDl3o4sK2igxPp_wBAz2vry_EHwv4yKQLq8CSZr75JQ130_head.
- NP748914.RAYDl3o4sK2igxPp_wBAz2vry_EHwv4yKQLq8CSZr75JQ130_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." NP748914.RAYDl3o4sK2igxPp_wBAz2vry_EHwv4yKQLq8CSZr75JQ130_provenance.
- NP748914.RAYDl3o4sK2igxPp_wBAz2vry_EHwv4yKQLq8CSZr75JQ130_assertion evidence source_evidence_literature NP748914.RAYDl3o4sK2igxPp_wBAz2vry_EHwv4yKQLq8CSZr75JQ130_provenance.
- NP748914.RAYDl3o4sK2igxPp_wBAz2vry_EHwv4yKQLq8CSZr75JQ130_assertion SIO_000772 15639189 NP748914.RAYDl3o4sK2igxPp_wBAz2vry_EHwv4yKQLq8CSZr75JQ130_provenance.
- NP748914.RAYDl3o4sK2igxPp_wBAz2vry_EHwv4yKQLq8CSZr75JQ130_assertion wasDerivedFrom befree-20150227 NP748914.RAYDl3o4sK2igxPp_wBAz2vry_EHwv4yKQLq8CSZr75JQ130_provenance.
- NP748914.RAYDl3o4sK2igxPp_wBAz2vry_EHwv4yKQLq8CSZr75JQ130_assertion wasGeneratedBy ECO_0000203 NP748914.RAYDl3o4sK2igxPp_wBAz2vry_EHwv4yKQLq8CSZr75JQ130_provenance.