Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP406128.RAh1cZOExeO6r9HKIxjATCCb7WoZK5W4Bc65aDHAT7fPg130_assertion> ?p ?o ?g. }
Showing items 1 to 6 of
6
with 100 items per page.
- NP406128.RAh1cZOExeO6r9HKIxjATCCb7WoZK5W4Bc65aDHAT7fPg130_assertion type Assertion NP406128.RAh1cZOExeO6r9HKIxjATCCb7WoZK5W4Bc65aDHAT7fPg130_head.
- NP406128.RAh1cZOExeO6r9HKIxjATCCb7WoZK5W4Bc65aDHAT7fPg130_assertion description "[Two of the most common clinical presentations, Leigh Syndrome and hypertrophic cardiomyopathy, have so far only been associated with mutations in SURF1 or SCO2 and COX15, respectively.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP406128.RAh1cZOExeO6r9HKIxjATCCb7WoZK5W4Bc65aDHAT7fPg130_provenance.
- NP406128.RAh1cZOExeO6r9HKIxjATCCb7WoZK5W4Bc65aDHAT7fPg130_assertion evidence source_evidence_literature NP406128.RAh1cZOExeO6r9HKIxjATCCb7WoZK5W4Bc65aDHAT7fPg130_provenance.
- NP406128.RAh1cZOExeO6r9HKIxjATCCb7WoZK5W4Bc65aDHAT7fPg130_assertion SIO_000772 12928484 NP406128.RAh1cZOExeO6r9HKIxjATCCb7WoZK5W4Bc65aDHAT7fPg130_provenance.
- NP406128.RAh1cZOExeO6r9HKIxjATCCb7WoZK5W4Bc65aDHAT7fPg130_assertion wasDerivedFrom befree-2016 NP406128.RAh1cZOExeO6r9HKIxjATCCb7WoZK5W4Bc65aDHAT7fPg130_provenance.
- NP406128.RAh1cZOExeO6r9HKIxjATCCb7WoZK5W4Bc65aDHAT7fPg130_assertion wasGeneratedBy ECO_0000203 NP406128.RAh1cZOExeO6r9HKIxjATCCb7WoZK5W4Bc65aDHAT7fPg130_provenance.