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- NP927388.RADp3FHIrBqlz__S4WPY1S6SjOQXKo2wUEMR48f_9iPT0130_assertion type Assertion NP927388.RADp3FHIrBqlz__S4WPY1S6SjOQXKo2wUEMR48f_9iPT0130_head.
- NP927388.RADp3FHIrBqlz__S4WPY1S6SjOQXKo2wUEMR48f_9iPT0130_assertion description "[Cerebrotendinous Xanthomatosis (CTX) is a rare autosomal recessive lipid storage disease caused by sterol 27-hydroxylase (CYP27) deficiency.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP927388.RADp3FHIrBqlz__S4WPY1S6SjOQXKo2wUEMR48f_9iPT0130_provenance.
- NP927388.RADp3FHIrBqlz__S4WPY1S6SjOQXKo2wUEMR48f_9iPT0130_assertion evidence source_evidence_literature NP927388.RADp3FHIrBqlz__S4WPY1S6SjOQXKo2wUEMR48f_9iPT0130_provenance.
- NP927388.RADp3FHIrBqlz__S4WPY1S6SjOQXKo2wUEMR48f_9iPT0130_assertion SIO_000772 21958693 NP927388.RADp3FHIrBqlz__S4WPY1S6SjOQXKo2wUEMR48f_9iPT0130_provenance.
- NP927388.RADp3FHIrBqlz__S4WPY1S6SjOQXKo2wUEMR48f_9iPT0130_assertion wasDerivedFrom befree-2016 NP927388.RADp3FHIrBqlz__S4WPY1S6SjOQXKo2wUEMR48f_9iPT0130_provenance.
- NP927388.RADp3FHIrBqlz__S4WPY1S6SjOQXKo2wUEMR48f_9iPT0130_assertion wasGeneratedBy ECO_0000203 NP927388.RADp3FHIrBqlz__S4WPY1S6SjOQXKo2wUEMR48f_9iPT0130_provenance.