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- NP323014.RATJCVCy-I1eNPtn2xw1l6yLuPCbfvKU9CAnEEhkKRHtw130_assertion type Assertion NP323014.RATJCVCy-I1eNPtn2xw1l6yLuPCbfvKU9CAnEEhkKRHtw130_head.
- NP323014.RATJCVCy-I1eNPtn2xw1l6yLuPCbfvKU9CAnEEhkKRHtw130_assertion description "[OPA1 mutations in patients with autosomal dominant optic atrophy and evidence for semi-dominant inheritance.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP323014.RATJCVCy-I1eNPtn2xw1l6yLuPCbfvKU9CAnEEhkKRHtw130_provenance.
- NP323014.RATJCVCy-I1eNPtn2xw1l6yLuPCbfvKU9CAnEEhkKRHtw130_assertion evidence source_evidence_literature NP323014.RATJCVCy-I1eNPtn2xw1l6yLuPCbfvKU9CAnEEhkKRHtw130_provenance.
- NP323014.RATJCVCy-I1eNPtn2xw1l6yLuPCbfvKU9CAnEEhkKRHtw130_assertion SIO_000772 11440988 NP323014.RATJCVCy-I1eNPtn2xw1l6yLuPCbfvKU9CAnEEhkKRHtw130_provenance.
- NP323014.RATJCVCy-I1eNPtn2xw1l6yLuPCbfvKU9CAnEEhkKRHtw130_assertion wasDerivedFrom befree-2016 NP323014.RATJCVCy-I1eNPtn2xw1l6yLuPCbfvKU9CAnEEhkKRHtw130_provenance.
- NP323014.RATJCVCy-I1eNPtn2xw1l6yLuPCbfvKU9CAnEEhkKRHtw130_assertion wasGeneratedBy ECO_0000203 NP323014.RATJCVCy-I1eNPtn2xw1l6yLuPCbfvKU9CAnEEhkKRHtw130_provenance.