Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP345679.RAYQeVSZewtkQ4mJoBiKFJQuoQtR5-AsEql3zvYRz_oxY130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP345679.RAYQeVSZewtkQ4mJoBiKFJQuoQtR5-AsEql3zvYRz_oxY130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP345679.RAYQeVSZewtkQ4mJoBiKFJQuoQtR5-AsEql3zvYRz_oxY130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP345679.RAYQeVSZewtkQ4mJoBiKFJQuoQtR5-AsEql3zvYRz_oxY130_provenance.
- NP345679.RAYQeVSZewtkQ4mJoBiKFJQuoQtR5-AsEql3zvYRz_oxY130_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." NP345679.RAYQeVSZewtkQ4mJoBiKFJQuoQtR5-AsEql3zvYRz_oxY130_provenance.
- NP345679.RAYQeVSZewtkQ4mJoBiKFJQuoQtR5-AsEql3zvYRz_oxY130_assertion evidence source_evidence_literature NP345679.RAYQeVSZewtkQ4mJoBiKFJQuoQtR5-AsEql3zvYRz_oxY130_provenance.
- NP345679.RAYQeVSZewtkQ4mJoBiKFJQuoQtR5-AsEql3zvYRz_oxY130_assertion SIO_000772 21958693 NP345679.RAYQeVSZewtkQ4mJoBiKFJQuoQtR5-AsEql3zvYRz_oxY130_provenance.
- NP345679.RAYQeVSZewtkQ4mJoBiKFJQuoQtR5-AsEql3zvYRz_oxY130_assertion wasDerivedFrom befree-20150227 NP345679.RAYQeVSZewtkQ4mJoBiKFJQuoQtR5-AsEql3zvYRz_oxY130_provenance.
- NP345679.RAYQeVSZewtkQ4mJoBiKFJQuoQtR5-AsEql3zvYRz_oxY130_assertion wasGeneratedBy ECO_0000203 NP345679.RAYQeVSZewtkQ4mJoBiKFJQuoQtR5-AsEql3zvYRz_oxY130_provenance.
- befree-20150227 importedOn "2015-02-27" NP345679.RAYQeVSZewtkQ4mJoBiKFJQuoQtR5-AsEql3zvYRz_oxY130_provenance.