Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP602666.RA8g7artWvm5mU-kv7gHMBpC0hlJJu-Fu58Pabxt6ek0Q130_assertion> ?p ?o ?g. }
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- NP602666.RA8g7artWvm5mU-kv7gHMBpC0hlJJu-Fu58Pabxt6ek0Q130_assertion type Assertion NP602666.RA8g7artWvm5mU-kv7gHMBpC0hlJJu-Fu58Pabxt6ek0Q130_head.
- NP602666.RA8g7artWvm5mU-kv7gHMBpC0hlJJu-Fu58Pabxt6ek0Q130_assertion description "[Although we initially focused on the mutation in POLG2, the mutation in OPA1 is more likely to explain the late-onset PEO and multisystem disorder in this patient.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP602666.RA8g7artWvm5mU-kv7gHMBpC0hlJJu-Fu58Pabxt6ek0Q130_provenance.
- NP602666.RA8g7artWvm5mU-kv7gHMBpC0hlJJu-Fu58Pabxt6ek0Q130_assertion evidence source_evidence_literature NP602666.RA8g7artWvm5mU-kv7gHMBpC0hlJJu-Fu58Pabxt6ek0Q130_provenance.
- NP602666.RA8g7artWvm5mU-kv7gHMBpC0hlJJu-Fu58Pabxt6ek0Q130_assertion SIO_000772 18195150 NP602666.RA8g7artWvm5mU-kv7gHMBpC0hlJJu-Fu58Pabxt6ek0Q130_provenance.
- NP602666.RA8g7artWvm5mU-kv7gHMBpC0hlJJu-Fu58Pabxt6ek0Q130_assertion wasDerivedFrom befree-20150227 NP602666.RA8g7artWvm5mU-kv7gHMBpC0hlJJu-Fu58Pabxt6ek0Q130_provenance.
- NP602666.RA8g7artWvm5mU-kv7gHMBpC0hlJJu-Fu58Pabxt6ek0Q130_assertion wasGeneratedBy ECO_0000203 NP602666.RA8g7artWvm5mU-kv7gHMBpC0hlJJu-Fu58Pabxt6ek0Q130_provenance.