Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP6066.RAIczhkx4R_DlqMWq-uDSglbfBzeyncFoEky03P1U95qA130_assertion> ?p ?o ?g. }
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- NP6066.RAIczhkx4R_DlqMWq-uDSglbfBzeyncFoEky03P1U95qA130_assertion type Assertion NP6066.RAIczhkx4R_DlqMWq-uDSglbfBzeyncFoEky03P1U95qA130_head.
- NP6066.RAIczhkx4R_DlqMWq-uDSglbfBzeyncFoEky03P1U95qA130_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." NP6066.RAIczhkx4R_DlqMWq-uDSglbfBzeyncFoEky03P1U95qA130_provenance.
- NP6066.RAIczhkx4R_DlqMWq-uDSglbfBzeyncFoEky03P1U95qA130_assertion evidence source_evidence_curated NP6066.RAIczhkx4R_DlqMWq-uDSglbfBzeyncFoEky03P1U95qA130_provenance.
- NP6066.RAIczhkx4R_DlqMWq-uDSglbfBzeyncFoEky03P1U95qA130_assertion SIO_000772 20080860 NP6066.RAIczhkx4R_DlqMWq-uDSglbfBzeyncFoEky03P1U95qA130_provenance.
- NP6066.RAIczhkx4R_DlqMWq-uDSglbfBzeyncFoEky03P1U95qA130_assertion wasDerivedFrom uniprot-2016 NP6066.RAIczhkx4R_DlqMWq-uDSglbfBzeyncFoEky03P1U95qA130_provenance.
- NP6066.RAIczhkx4R_DlqMWq-uDSglbfBzeyncFoEky03P1U95qA130_assertion wasGeneratedBy ECO_0000218 NP6066.RAIczhkx4R_DlqMWq-uDSglbfBzeyncFoEky03P1U95qA130_provenance.