Nanopublications LDF server

Matches in Nanopublications for { ?s ?p "[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."@en ?g. }

• NP649939.RAXEOJqVPWtqJGYiVLkG-2xcX9Pf_NbC_vZZwUQ1ln0q0130_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." NP649939.RAXEOJqVPWtqJGYiVLkG-2xcX9Pf_NbC_vZZwUQ1ln0q0130_provenance.
• NP649937.RAvNdf37893UTCUA3dEKvUFnoPTvK8yzXt5hIKJwQI7Po130_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." NP649937.RAvNdf37893UTCUA3dEKvUFnoPTvK8yzXt5hIKJwQI7Po130_provenance.
• NP602693.RAMnKI7X8QhPJWU5i6bTOIbgryAPB4BI4kr3i3HbONJr0130_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." NP602693.RAMnKI7X8QhPJWU5i6bTOIbgryAPB4BI4kr3i3HbONJr0130_provenance.
• 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.
• NP649936.RAP5kM-4VqPYF7YgR173kif06Y2VeGtuo7adwmQDkUBSk130_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." NP649936.RAP5kM-4VqPYF7YgR173kif06Y2VeGtuo7adwmQDkUBSk130_provenance.
• NP833587.RAw_W3wca2LvIAN8FAusw54w-11wVm8IjkFS4zejePF3k130_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." NP833587.RAw_W3wca2LvIAN8FAusw54w-11wVm8IjkFS4zejePF3k130_provenance.
• NP833540.RANV4O3U8mNptCeI0yHDdM1rYL8jLyCymMwQ9sI5ft3yA130_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." NP833540.RANV4O3U8mNptCeI0yHDdM1rYL8jLyCymMwQ9sI5ft3yA130_provenance.
• NP649938.RA35PtS63SPqloakVzogErGBXy-AT6wPUj95r5wnb_Acg130_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." NP649938.RA35PtS63SPqloakVzogErGBXy-AT6wPUj95r5wnb_Acg130_provenance.
• NP649942.RA5y7J6IJj0ERK4ZalZRQgDvMm1B8jJHoxT2v8PmUCDmU130_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." NP649942.RA5y7J6IJj0ERK4ZalZRQgDvMm1B8jJHoxT2v8PmUCDmU130_provenance.
• NP863369.RA1wkm770I41U1pP4SgS_P3X6j5GYMwpstDD4nttQr8p0130_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." NP863369.RA1wkm770I41U1pP4SgS_P3X6j5GYMwpstDD4nttQr8p0130_provenance.