Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP927388.RADp3FHIrBqlz__S4WPY1S6SjOQXKo2wUEMR48f_9iPT0130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP927388.RADp3FHIrBqlz__S4WPY1S6SjOQXKo2wUEMR48f_9iPT0130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP927388.RADp3FHIrBqlz__S4WPY1S6SjOQXKo2wUEMR48f_9iPT0130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP927388.RADp3FHIrBqlz__S4WPY1S6SjOQXKo2wUEMR48f_9iPT0130_provenance.
- 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.
- befree-2016 importedOn "2016-02-19" NP927388.RADp3FHIrBqlz__S4WPY1S6SjOQXKo2wUEMR48f_9iPT0130_provenance.