Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP620990.RAVN2dsP4g26hZn3lGLmr_UlE1uM5QSYx6CAtFa90V_0M130_assertion> ?p ?o ?g. }
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- NP620990.RAVN2dsP4g26hZn3lGLmr_UlE1uM5QSYx6CAtFa90V_0M130_assertion type Assertion NP620990.RAVN2dsP4g26hZn3lGLmr_UlE1uM5QSYx6CAtFa90V_0M130_head.
- NP620990.RAVN2dsP4g26hZn3lGLmr_UlE1uM5QSYx6CAtFa90V_0M130_assertion description "[Cytochrome b mutations in Leber hereditary optic neuropathy.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP620990.RAVN2dsP4g26hZn3lGLmr_UlE1uM5QSYx6CAtFa90V_0M130_provenance.
- NP620990.RAVN2dsP4g26hZn3lGLmr_UlE1uM5QSYx6CAtFa90V_0M130_assertion evidence source_evidence_literature NP620990.RAVN2dsP4g26hZn3lGLmr_UlE1uM5QSYx6CAtFa90V_0M130_provenance.
- NP620990.RAVN2dsP4g26hZn3lGLmr_UlE1uM5QSYx6CAtFa90V_0M130_assertion SIO_000772 1764087 NP620990.RAVN2dsP4g26hZn3lGLmr_UlE1uM5QSYx6CAtFa90V_0M130_provenance.
- NP620990.RAVN2dsP4g26hZn3lGLmr_UlE1uM5QSYx6CAtFa90V_0M130_assertion wasDerivedFrom befree-2016 NP620990.RAVN2dsP4g26hZn3lGLmr_UlE1uM5QSYx6CAtFa90V_0M130_provenance.
- NP620990.RAVN2dsP4g26hZn3lGLmr_UlE1uM5QSYx6CAtFa90V_0M130_assertion wasGeneratedBy ECO_0000203 NP620990.RAVN2dsP4g26hZn3lGLmr_UlE1uM5QSYx6CAtFa90V_0M130_provenance.