Nanopublications LDF server

Matches in Nanopublications for { ?s ?p "[Heterozygous optic atrophy type1 (OPA1) mutations are responsible for dominant optic atrophy, and the down regulation of OPA1 expression in patients with Leber hereditary optic neuropathy may imply that Opa1 protein levels in mitochondria play a role in other spontaneous optic neuropathies as well.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ?g. }

• NP271555.RAMyIc2WxYurE7mz1WwiL5a1QNJairkA3HezCKNagXLk0130_assertion description "[Heterozygous optic atrophy type1 (OPA1) mutations are responsible for dominant optic atrophy, and the down regulation of OPA1 expression in patients with Leber hereditary optic neuropathy may imply that Opa1 protein levels in mitochondria play a role in other spontaneous optic neuropathies as well.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP271555.RAMyIc2WxYurE7mz1WwiL5a1QNJairkA3HezCKNagXLk0130_provenance.
• NP243661.RAvejiFrqZjt13sDKFk10q03HywuwC6xUPx83sBj7jjJ4130_assertion description "[Heterozygous optic atrophy type1 (OPA1) mutations are responsible for dominant optic atrophy, and the down regulation of OPA1 expression in patients with Leber hereditary optic neuropathy may imply that Opa1 protein levels in mitochondria play a role in other spontaneous optic neuropathies as well.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP243661.RAvejiFrqZjt13sDKFk10q03HywuwC6xUPx83sBj7jjJ4130_provenance.
• NP835831.RA3iPLDMsgZKDukqlvgCty7dI4Hk3leD9VDwbfpYNKYZE130_assertion description "[Heterozygous optic atrophy type1 (OPA1) mutations are responsible for dominant optic atrophy, and the down regulation of OPA1 expression in patients with Leber hereditary optic neuropathy may imply that Opa1 protein levels in mitochondria play a role in other spontaneous optic neuropathies as well.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP835831.RA3iPLDMsgZKDukqlvgCty7dI4Hk3leD9VDwbfpYNKYZE130_provenance.
• NP602615.RAdcMVdkvn0YOOVYo9eWutP0DA-ZzEgHPx3QZvsb-JBWQ130_assertion description "[Heterozygous optic atrophy type1 (OPA1) mutations are responsible for dominant optic atrophy, and the down regulation of OPA1 expression in patients with Leber hereditary optic neuropathy may imply that Opa1 protein levels in mitochondria play a role in other spontaneous optic neuropathies as well.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP602615.RAdcMVdkvn0YOOVYo9eWutP0DA-ZzEgHPx3QZvsb-JBWQ130_provenance.
• NP602714.RAYSn-YfwJJVCVWHi25PVpolnDh-bSZx_MApAbpz2Ieks130_assertion description "[Heterozygous optic atrophy type1 (OPA1) mutations are responsible for dominant optic atrophy, and the down regulation of OPA1 expression in patients with Leber hereditary optic neuropathy may imply that Opa1 protein levels in mitochondria play a role in other spontaneous optic neuropathies as well.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP602714.RAYSn-YfwJJVCVWHi25PVpolnDh-bSZx_MApAbpz2Ieks130_provenance.
• assertion description "[Heterozygous optic atrophy type1 (OPA1) mutations are responsible for dominant optic atrophy, and the down regulation of OPA1 expression in patients with Leber hereditary optic neuropathy may imply that Opa1 protein levels in mitochondria play a role in other spontaneous optic neuropathies as well.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
• assertion description "[Heterozygous optic atrophy type1 (OPA1) mutations are responsible for dominant optic atrophy, and the down regulation of OPA1 expression in patients with Leber hereditary optic neuropathy may imply that Opa1 protein levels in mitochondria play a role in other spontaneous optic neuropathies as well.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
• NP892504.RASh1I4hQl1Ae89SzhPRxLP-QnRsVorrAbmf59_KY73lQ130_assertion description "[Heterozygous optic atrophy type1 (OPA1) mutations are responsible for dominant optic atrophy, and the down regulation of OPA1 expression in patients with Leber hereditary optic neuropathy may imply that Opa1 protein levels in mitochondria play a role in other spontaneous optic neuropathies as well.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP892504.RASh1I4hQl1Ae89SzhPRxLP-QnRsVorrAbmf59_KY73lQ130_provenance.
• NP892505.RAcKsz2F3vGgWSIjDV3boFFTtH5bEjnKKxteo2sSaHp6o130_assertion description "[Heterozygous optic atrophy type1 (OPA1) mutations are responsible for dominant optic atrophy, and the down regulation of OPA1 expression in patients with Leber hereditary optic neuropathy may imply that Opa1 protein levels in mitochondria play a role in other spontaneous optic neuropathies as well.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP892505.RAcKsz2F3vGgWSIjDV3boFFTtH5bEjnKKxteo2sSaHp6o130_provenance.
• NP892508.RATi9rM8qSsEiRK92VU4eLn2Dj1BKVM_tUCnLqVptCsHQ130_assertion description "[Heterozygous optic atrophy type1 (OPA1) mutations are responsible for dominant optic atrophy, and the down regulation of OPA1 expression in patients with Leber hereditary optic neuropathy may imply that Opa1 protein levels in mitochondria play a role in other spontaneous optic neuropathies as well.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP892508.RATi9rM8qSsEiRK92VU4eLn2Dj1BKVM_tUCnLqVptCsHQ130_provenance.
• NP892500.RAFuKvuCv6nS3DEb6BIR_8kizwvwg3khZ6KcJA3ftqb2A130_assertion description "[Heterozygous optic atrophy type1 (OPA1) mutations are responsible for dominant optic atrophy, and the down regulation of OPA1 expression in patients with Leber hereditary optic neuropathy may imply that Opa1 protein levels in mitochondria play a role in other spontaneous optic neuropathies as well.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP892500.RAFuKvuCv6nS3DEb6BIR_8kizwvwg3khZ6KcJA3ftqb2A130_provenance.
• NP892501.RANsYA1RHesHCEO-P-2Bvuv3GouYMfzPsNGW8D16EtlDI130_assertion description "[Heterozygous optic atrophy type1 (OPA1) mutations are responsible for dominant optic atrophy, and the down regulation of OPA1 expression in patients with Leber hereditary optic neuropathy may imply that Opa1 protein levels in mitochondria play a role in other spontaneous optic neuropathies as well.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP892501.RANsYA1RHesHCEO-P-2Bvuv3GouYMfzPsNGW8D16EtlDI130_provenance.
• NP833466.RA6-y_AWRS_aJV0WLCWzXBEB3nb1xkxSo0sFQ--B0QaRk130_assertion description "[Heterozygous optic atrophy type1 (OPA1) mutations are responsible for dominant optic atrophy, and the down regulation of OPA1 expression in patients with Leber hereditary optic neuropathy may imply that Opa1 protein levels in mitochondria play a role in other spontaneous optic neuropathies as well.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP833466.RA6-y_AWRS_aJV0WLCWzXBEB3nb1xkxSo0sFQ--B0QaRk130_provenance.
• NP833615.RAGFd6ONwk4CYoFKVRhwk4uRHc2unOn7pxI5MCvbkV2HY130_assertion description "[Heterozygous optic atrophy type1 (OPA1) mutations are responsible for dominant optic atrophy, and the down regulation of OPA1 expression in patients with Leber hereditary optic neuropathy may imply that Opa1 protein levels in mitochondria play a role in other spontaneous optic neuropathies as well.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP833615.RAGFd6ONwk4CYoFKVRhwk4uRHc2unOn7pxI5MCvbkV2HY130_provenance.
• NP892503.RAxz04nS0Xk5oTR9Jc0qjdnd4Sxutt8ygQRgfyCDu2NnY130_assertion description "[Heterozygous optic atrophy type1 (OPA1) mutations are responsible for dominant optic atrophy, and the down regulation of OPA1 expression in patients with Leber hereditary optic neuropathy may imply that Opa1 protein levels in mitochondria play a role in other spontaneous optic neuropathies as well.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP892503.RAxz04nS0Xk5oTR9Jc0qjdnd4Sxutt8ygQRgfyCDu2NnY130_provenance.