Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP31797.RACLBeZuRB0wwOlHOU6l-9RW0e1QUYrdpTJnVZMCVVns0130_assertion> ?p ?o ?g. }
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- NP31797.RACLBeZuRB0wwOlHOU6l-9RW0e1QUYrdpTJnVZMCVVns0130_assertion type Assertion NP31797.RACLBeZuRB0wwOlHOU6l-9RW0e1QUYrdpTJnVZMCVVns0130_head.
- NP31797.RACLBeZuRB0wwOlHOU6l-9RW0e1QUYrdpTJnVZMCVVns0130_assertion wasGeneratedBy ECO_0000218 NP31797.RACLBeZuRB0wwOlHOU6l-9RW0e1QUYrdpTJnVZMCVVns0130_provenance.
- NP31797.RACLBeZuRB0wwOlHOU6l-9RW0e1QUYrdpTJnVZMCVVns0130_assertion wasDerivedFrom ctd_human-20150221 NP31797.RACLBeZuRB0wwOlHOU6l-9RW0e1QUYrdpTJnVZMCVVns0130_provenance.
- NP31797.RACLBeZuRB0wwOlHOU6l-9RW0e1QUYrdpTJnVZMCVVns0130_assertion SIO_000772 21725307 NP31797.RACLBeZuRB0wwOlHOU6l-9RW0e1QUYrdpTJnVZMCVVns0130_provenance.
- NP31797.RACLBeZuRB0wwOlHOU6l-9RW0e1QUYrdpTJnVZMCVVns0130_assertion evidence source_evidence_curated NP31797.RACLBeZuRB0wwOlHOU6l-9RW0e1QUYrdpTJnVZMCVVns0130_provenance.
- NP31797.RACLBeZuRB0wwOlHOU6l-9RW0e1QUYrdpTJnVZMCVVns0130_assertion description "[Consistent with a shared function for complex components, we identified a mutation in TCTN1 that causes Joubert syndrome.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP31797.RACLBeZuRB0wwOlHOU6l-9RW0e1QUYrdpTJnVZMCVVns0130_provenance.