Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP223118.RAp-gpCIdt7FoxhdHO4su_r6Y2rOsVjJqU6qAiLgyVZpE130_assertion> ?p ?o ?g. }
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- NP223118.RAp-gpCIdt7FoxhdHO4su_r6Y2rOsVjJqU6qAiLgyVZpE130_assertion type Assertion NP223118.RAp-gpCIdt7FoxhdHO4su_r6Y2rOsVjJqU6qAiLgyVZpE130_head.
- NP223118.RAp-gpCIdt7FoxhdHO4su_r6Y2rOsVjJqU6qAiLgyVZpE130_assertion wasGeneratedBy ECO_0000203 NP223118.RAp-gpCIdt7FoxhdHO4su_r6Y2rOsVjJqU6qAiLgyVZpE130_provenance.
- NP223118.RAp-gpCIdt7FoxhdHO4su_r6Y2rOsVjJqU6qAiLgyVZpE130_assertion wasDerivedFrom befree-20140225 NP223118.RAp-gpCIdt7FoxhdHO4su_r6Y2rOsVjJqU6qAiLgyVZpE130_provenance.
- NP223118.RAp-gpCIdt7FoxhdHO4su_r6Y2rOsVjJqU6qAiLgyVZpE130_assertion SIO_000772 18188677 NP223118.RAp-gpCIdt7FoxhdHO4su_r6Y2rOsVjJqU6qAiLgyVZpE130_provenance.
- NP223118.RAp-gpCIdt7FoxhdHO4su_r6Y2rOsVjJqU6qAiLgyVZpE130_assertion evidence source_evidence_literature NP223118.RAp-gpCIdt7FoxhdHO4su_r6Y2rOsVjJqU6qAiLgyVZpE130_provenance.
- NP223118.RAp-gpCIdt7FoxhdHO4su_r6Y2rOsVjJqU6qAiLgyVZpE130_assertion description "[Type III galactosaemia is a hereditary disease caused by reduced activity in the Leloir pathway enzyme, UDP-galactose 4'-epimerase (GALE).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP223118.RAp-gpCIdt7FoxhdHO4su_r6Y2rOsVjJqU6qAiLgyVZpE130_provenance.