Nanopublications LDF server

Matches in Nanopublications for { ?s ?p "[Sensory ataxia with neuropathy, dysarthria and ophthalmoparesis represent the clinical triad of SANDO, a specific mitochondrial phenotype first reported in 1997 in association with multiple mitochondrial DNA deletions and mutations in POLG1 or more rarely in the C10orf2 (twinkle-helicase) gene.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ?g. }

• NP769952.RAb5lx-lxNKY522Xdum2T_vSaifGZqXgJcc3YRr4WIo_U130_assertion description "[Sensory ataxia with neuropathy, dysarthria and ophthalmoparesis represent the clinical triad of SANDO, a specific mitochondrial phenotype first reported in 1997 in association with multiple mitochondrial DNA deletions and mutations in POLG1 or more rarely in the C10orf2 (twinkle-helicase) gene.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP769952.RAb5lx-lxNKY522Xdum2T_vSaifGZqXgJcc3YRr4WIo_U130_provenance.
• NP648151.RAeODAqpEFtkrEovR5MnlBhFD_tJT5_LzkoGDxlZvNPKE130_assertion description "[Sensory ataxia with neuropathy, dysarthria and ophthalmoparesis represent the clinical triad of SANDO, a specific mitochondrial phenotype first reported in 1997 in association with multiple mitochondrial DNA deletions and mutations in POLG1 or more rarely in the C10orf2 (twinkle-helicase) gene.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP648151.RAeODAqpEFtkrEovR5MnlBhFD_tJT5_LzkoGDxlZvNPKE130_provenance.
• NP493110.RATi9C6QF0Jmle_PhyVLu3NAuixZt0QQ0GvlAJwjfoZ_I130_assertion description "[Sensory ataxia with neuropathy, dysarthria and ophthalmoparesis represent the clinical triad of SANDO, a specific mitochondrial phenotype first reported in 1997 in association with multiple mitochondrial DNA deletions and mutations in POLG1 or more rarely in the C10orf2 (twinkle-helicase) gene.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP493110.RATi9C6QF0Jmle_PhyVLu3NAuixZt0QQ0GvlAJwjfoZ_I130_provenance.
• NP565111.RAC8aKhRlpZia3majpH9xj8F2mx_6qUbxTY8JwOzpyalM130_assertion description "[Sensory ataxia with neuropathy, dysarthria and ophthalmoparesis represent the clinical triad of SANDO, a specific mitochondrial phenotype first reported in 1997 in association with multiple mitochondrial DNA deletions and mutations in POLG1 or more rarely in the C10orf2 (twinkle-helicase) gene.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP565111.RAC8aKhRlpZia3majpH9xj8F2mx_6qUbxTY8JwOzpyalM130_provenance.
• NP923888.RAfIw851s39KJtj10MnBVoycwcblygKmRY9olCpcZqMtU130_assertion description "[Sensory ataxia with neuropathy, dysarthria and ophthalmoparesis represent the clinical triad of SANDO, a specific mitochondrial phenotype first reported in 1997 in association with multiple mitochondrial DNA deletions and mutations in POLG1 or more rarely in the C10orf2 (twinkle-helicase) gene.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP923888.RAfIw851s39KJtj10MnBVoycwcblygKmRY9olCpcZqMtU130_provenance.
• NP928718.RA9Ikhy7lMHB2bszdAHrruZSUDq0QC_SUB9Unab0OTolo130_assertion description "[Sensory ataxia with neuropathy, dysarthria and ophthalmoparesis represent the clinical triad of SANDO, a specific mitochondrial phenotype first reported in 1997 in association with multiple mitochondrial DNA deletions and mutations in POLG1 or more rarely in the C10orf2 (twinkle-helicase) gene.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP928718.RA9Ikhy7lMHB2bszdAHrruZSUDq0QC_SUB9Unab0OTolo130_provenance.
• NP565109.RAwM0XAPLn2M8vtAIzBt_i6hzzdIcRV5pXXM2ZZ-rdeMg130_assertion description "[Sensory ataxia with neuropathy, dysarthria and ophthalmoparesis represent the clinical triad of SANDO, a specific mitochondrial phenotype first reported in 1997 in association with multiple mitochondrial DNA deletions and mutations in POLG1 or more rarely in the C10orf2 (twinkle-helicase) gene.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP565109.RAwM0XAPLn2M8vtAIzBt_i6hzzdIcRV5pXXM2ZZ-rdeMg130_provenance.
• NP565110.RA3b2TGV2JWf3yz3bRSrsevqYghwaBGDSN2p5qJW2hSuU130_assertion description "[Sensory ataxia with neuropathy, dysarthria and ophthalmoparesis represent the clinical triad of SANDO, a specific mitochondrial phenotype first reported in 1997 in association with multiple mitochondrial DNA deletions and mutations in POLG1 or more rarely in the C10orf2 (twinkle-helicase) gene.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP565110.RA3b2TGV2JWf3yz3bRSrsevqYghwaBGDSN2p5qJW2hSuU130_provenance.
• assertion description "[Sensory ataxia with neuropathy, dysarthria and ophthalmoparesis represent the clinical triad of SANDO, a specific mitochondrial phenotype first reported in 1997 in association with multiple mitochondrial DNA deletions and mutations in POLG1 or more rarely in the C10orf2 (twinkle-helicase) gene.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
• assertion description "[Sensory ataxia with neuropathy, dysarthria and ophthalmoparesis represent the clinical triad of SANDO, a specific mitochondrial phenotype first reported in 1997 in association with multiple mitochondrial DNA deletions and mutations in POLG1 or more rarely in the C10orf2 (twinkle-helicase) gene.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
• assertion description "[Sensory ataxia with neuropathy, dysarthria and ophthalmoparesis represent the clinical triad of SANDO, a specific mitochondrial phenotype first reported in 1997 in association with multiple mitochondrial DNA deletions and mutations in POLG1 or more rarely in the C10orf2 (twinkle-helicase) gene.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
• NP633600.RAtlFQIKoQUie5F6YVcG_IPco6qmY7ptWc49NeeerHUoo130_assertion description "[Sensory ataxia with neuropathy, dysarthria and ophthalmoparesis represent the clinical triad of SANDO, a specific mitochondrial phenotype first reported in 1997 in association with multiple mitochondrial DNA deletions and mutations in POLG1 or more rarely in the C10orf2 (twinkle-helicase) gene.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP633600.RAtlFQIKoQUie5F6YVcG_IPco6qmY7ptWc49NeeerHUoo130_provenance.