Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP879458.RAqK49aS9QLF2LS7YH0jmL_-lmt_NzSlfptpq9OE7P9Uw130_assertion> ?p ?o ?g. }
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- NP879458.RAqK49aS9QLF2LS7YH0jmL_-lmt_NzSlfptpq9OE7P9Uw130_assertion type Assertion NP879458.RAqK49aS9QLF2LS7YH0jmL_-lmt_NzSlfptpq9OE7P9Uw130_head.
- NP879458.RAqK49aS9QLF2LS7YH0jmL_-lmt_NzSlfptpq9OE7P9Uw130_assertion description "[Mutations in tripeptidyl-peptidase I (TPP I) underlie the classic late-infantile form of neuronal ceroid lipofuscinoses (CLN2), the most common neurodegenerative disorders of childhood.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP879458.RAqK49aS9QLF2LS7YH0jmL_-lmt_NzSlfptpq9OE7P9Uw130_provenance.
- NP879458.RAqK49aS9QLF2LS7YH0jmL_-lmt_NzSlfptpq9OE7P9Uw130_assertion evidence source_evidence_literature NP879458.RAqK49aS9QLF2LS7YH0jmL_-lmt_NzSlfptpq9OE7P9Uw130_provenance.
- NP879458.RAqK49aS9QLF2LS7YH0jmL_-lmt_NzSlfptpq9OE7P9Uw130_assertion SIO_000772 16895480 NP879458.RAqK49aS9QLF2LS7YH0jmL_-lmt_NzSlfptpq9OE7P9Uw130_provenance.
- NP879458.RAqK49aS9QLF2LS7YH0jmL_-lmt_NzSlfptpq9OE7P9Uw130_assertion wasDerivedFrom befree-20140225 NP879458.RAqK49aS9QLF2LS7YH0jmL_-lmt_NzSlfptpq9OE7P9Uw130_provenance.
- NP879458.RAqK49aS9QLF2LS7YH0jmL_-lmt_NzSlfptpq9OE7P9Uw130_assertion wasGeneratedBy ECO_0000203 NP879458.RAqK49aS9QLF2LS7YH0jmL_-lmt_NzSlfptpq9OE7P9Uw130_provenance.