Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP787616.RALj4RFE8r9kYJdLlPvlqOGnpsQRUMhTDVC88tr7mDEuA130_assertion> ?p ?o ?g. }
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- NP787616.RALj4RFE8r9kYJdLlPvlqOGnpsQRUMhTDVC88tr7mDEuA130_assertion type Assertion NP787616.RALj4RFE8r9kYJdLlPvlqOGnpsQRUMhTDVC88tr7mDEuA130_head.
- NP787616.RALj4RFE8r9kYJdLlPvlqOGnpsQRUMhTDVC88tr7mDEuA130_assertion description "[Phenotype-genotype correlations of 13 rare CYP21A2 mutations detected in 46 patients affected with 21-hydroxylase deficiency and in one carrier.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP787616.RALj4RFE8r9kYJdLlPvlqOGnpsQRUMhTDVC88tr7mDEuA130_provenance.
- NP787616.RALj4RFE8r9kYJdLlPvlqOGnpsQRUMhTDVC88tr7mDEuA130_assertion evidence source_evidence_literature NP787616.RALj4RFE8r9kYJdLlPvlqOGnpsQRUMhTDVC88tr7mDEuA130_provenance.
- NP787616.RALj4RFE8r9kYJdLlPvlqOGnpsQRUMhTDVC88tr7mDEuA130_assertion SIO_000772 20080860 NP787616.RALj4RFE8r9kYJdLlPvlqOGnpsQRUMhTDVC88tr7mDEuA130_provenance.
- NP787616.RALj4RFE8r9kYJdLlPvlqOGnpsQRUMhTDVC88tr7mDEuA130_assertion wasDerivedFrom befree-2016 NP787616.RALj4RFE8r9kYJdLlPvlqOGnpsQRUMhTDVC88tr7mDEuA130_provenance.
- NP787616.RALj4RFE8r9kYJdLlPvlqOGnpsQRUMhTDVC88tr7mDEuA130_assertion wasGeneratedBy ECO_0000203 NP787616.RALj4RFE8r9kYJdLlPvlqOGnpsQRUMhTDVC88tr7mDEuA130_provenance.