Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP445714.RAmNTcvA2W1XSjUZ6TZ35VpdOyISZuryHO4yR-Fp8Ag_Q130_assertion> ?p ?o ?g. }
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- NP445714.RAmNTcvA2W1XSjUZ6TZ35VpdOyISZuryHO4yR-Fp8Ag_Q130_assertion type Assertion NP445714.RAmNTcvA2W1XSjUZ6TZ35VpdOyISZuryHO4yR-Fp8Ag_Q130_head.
- NP445714.RAmNTcvA2W1XSjUZ6TZ35VpdOyISZuryHO4yR-Fp8Ag_Q130_assertion description "[The ND1 subunit gene of the mitochondrial NADH-ubiquinone oxidoreductase (complex I) is a hot spot for mutations causing Leber hereditary optic neuropathy and several mutations causing the mitochondrial encephalopathy, lactic acidosis and stroke-like episodes syndrome (MELAS).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP445714.RAmNTcvA2W1XSjUZ6TZ35VpdOyISZuryHO4yR-Fp8Ag_Q130_provenance.
- NP445714.RAmNTcvA2W1XSjUZ6TZ35VpdOyISZuryHO4yR-Fp8Ag_Q130_assertion evidence source_evidence_literature NP445714.RAmNTcvA2W1XSjUZ6TZ35VpdOyISZuryHO4yR-Fp8Ag_Q130_provenance.
- NP445714.RAmNTcvA2W1XSjUZ6TZ35VpdOyISZuryHO4yR-Fp8Ag_Q130_assertion SIO_000772 16849371 NP445714.RAmNTcvA2W1XSjUZ6TZ35VpdOyISZuryHO4yR-Fp8Ag_Q130_provenance.
- NP445714.RAmNTcvA2W1XSjUZ6TZ35VpdOyISZuryHO4yR-Fp8Ag_Q130_assertion wasDerivedFrom befree-20140225 NP445714.RAmNTcvA2W1XSjUZ6TZ35VpdOyISZuryHO4yR-Fp8Ag_Q130_provenance.
- NP445714.RAmNTcvA2W1XSjUZ6TZ35VpdOyISZuryHO4yR-Fp8Ag_Q130_assertion wasGeneratedBy ECO_0000203 NP445714.RAmNTcvA2W1XSjUZ6TZ35VpdOyISZuryHO4yR-Fp8Ag_Q130_provenance.