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- NP373884.RAV9nuzfFS2NpE1W_q2jkH4KKQ72bBdbEFdXkr8hC9E3o130_assertion type Assertion NP373884.RAV9nuzfFS2NpE1W_q2jkH4KKQ72bBdbEFdXkr8hC9E3o130_head.
- NP373884.RAV9nuzfFS2NpE1W_q2jkH4KKQ72bBdbEFdXkr8hC9E3o130_assertion wasGeneratedBy ECO_0000203 NP373884.RAV9nuzfFS2NpE1W_q2jkH4KKQ72bBdbEFdXkr8hC9E3o130_provenance.
- NP373884.RAV9nuzfFS2NpE1W_q2jkH4KKQ72bBdbEFdXkr8hC9E3o130_assertion wasDerivedFrom befree-20140225 NP373884.RAV9nuzfFS2NpE1W_q2jkH4KKQ72bBdbEFdXkr8hC9E3o130_provenance.
- NP373884.RAV9nuzfFS2NpE1W_q2jkH4KKQ72bBdbEFdXkr8hC9E3o130_assertion SIO_000772 23583749 NP373884.RAV9nuzfFS2NpE1W_q2jkH4KKQ72bBdbEFdXkr8hC9E3o130_provenance.
- NP373884.RAV9nuzfFS2NpE1W_q2jkH4KKQ72bBdbEFdXkr8hC9E3o130_assertion evidence source_evidence_literature NP373884.RAV9nuzfFS2NpE1W_q2jkH4KKQ72bBdbEFdXkr8hC9E3o130_provenance.
- NP373884.RAV9nuzfFS2NpE1W_q2jkH4KKQ72bBdbEFdXkr8hC9E3o130_assertion description "[Type I galactosemia is a genetic disorder that is caused by the impairment of galactose-1-phosphate uridylyltransferase (GALT; EC 2.7.7.12).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP373884.RAV9nuzfFS2NpE1W_q2jkH4KKQ72bBdbEFdXkr8hC9E3o130_provenance.