Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP477649.RAafLmaOoz3pqt7QjYrYpLIUNiJeKt2N_RyJ6rgl9uasM130_assertion> ?p ?o ?g. }
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- NP477649.RAafLmaOoz3pqt7QjYrYpLIUNiJeKt2N_RyJ6rgl9uasM130_assertion type Assertion NP477649.RAafLmaOoz3pqt7QjYrYpLIUNiJeKt2N_RyJ6rgl9uasM130_head.
- NP477649.RAafLmaOoz3pqt7QjYrYpLIUNiJeKt2N_RyJ6rgl9uasM130_assertion description "[Subsequent studies demonstrated that this mutation is present in one-half of all CG1 patients and correlates with the Zellweger syndrome phenotype.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP477649.RAafLmaOoz3pqt7QjYrYpLIUNiJeKt2N_RyJ6rgl9uasM130_provenance.
- NP477649.RAafLmaOoz3pqt7QjYrYpLIUNiJeKt2N_RyJ6rgl9uasM130_assertion evidence source_evidence_literature NP477649.RAafLmaOoz3pqt7QjYrYpLIUNiJeKt2N_RyJ6rgl9uasM130_provenance.
- NP477649.RAafLmaOoz3pqt7QjYrYpLIUNiJeKt2N_RyJ6rgl9uasM130_assertion SIO_000772 10447258 NP477649.RAafLmaOoz3pqt7QjYrYpLIUNiJeKt2N_RyJ6rgl9uasM130_provenance.
- NP477649.RAafLmaOoz3pqt7QjYrYpLIUNiJeKt2N_RyJ6rgl9uasM130_assertion wasDerivedFrom befree-20140225 NP477649.RAafLmaOoz3pqt7QjYrYpLIUNiJeKt2N_RyJ6rgl9uasM130_provenance.
- NP477649.RAafLmaOoz3pqt7QjYrYpLIUNiJeKt2N_RyJ6rgl9uasM130_assertion wasGeneratedBy ECO_0000203 NP477649.RAafLmaOoz3pqt7QjYrYpLIUNiJeKt2N_RyJ6rgl9uasM130_provenance.