Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP615229.RAIP49nQMtD4WnwLbDBMheVC5eVkRVXp-SGuvlYzK_zIA130_assertion> ?p ?o ?g. }
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- NP615229.RAIP49nQMtD4WnwLbDBMheVC5eVkRVXp-SGuvlYzK_zIA130_assertion type Assertion NP615229.RAIP49nQMtD4WnwLbDBMheVC5eVkRVXp-SGuvlYzK_zIA130_head.
- NP615229.RAIP49nQMtD4WnwLbDBMheVC5eVkRVXp-SGuvlYzK_zIA130_assertion description "[Cerebrotendinous xanthomatosis (CTX) is an autosomal recessive lipid storage disease caused by mutations in the cytochrome P450(27) (CYP27) gene.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP615229.RAIP49nQMtD4WnwLbDBMheVC5eVkRVXp-SGuvlYzK_zIA130_provenance.
- NP615229.RAIP49nQMtD4WnwLbDBMheVC5eVkRVXp-SGuvlYzK_zIA130_assertion evidence source_evidence_literature NP615229.RAIP49nQMtD4WnwLbDBMheVC5eVkRVXp-SGuvlYzK_zIA130_provenance.
- NP615229.RAIP49nQMtD4WnwLbDBMheVC5eVkRVXp-SGuvlYzK_zIA130_assertion SIO_000772 8728324 NP615229.RAIP49nQMtD4WnwLbDBMheVC5eVkRVXp-SGuvlYzK_zIA130_provenance.
- NP615229.RAIP49nQMtD4WnwLbDBMheVC5eVkRVXp-SGuvlYzK_zIA130_assertion wasDerivedFrom befree-20140225 NP615229.RAIP49nQMtD4WnwLbDBMheVC5eVkRVXp-SGuvlYzK_zIA130_provenance.
- NP615229.RAIP49nQMtD4WnwLbDBMheVC5eVkRVXp-SGuvlYzK_zIA130_assertion wasGeneratedBy ECO_0000203 NP615229.RAIP49nQMtD4WnwLbDBMheVC5eVkRVXp-SGuvlYzK_zIA130_provenance.