Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP865948.RA4Qe8v95HT5GuSrE0AoZDV1gZnya3LxsE-teNEtbheLs130_assertion> ?p ?o ?g. }
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- NP865948.RA4Qe8v95HT5GuSrE0AoZDV1gZnya3LxsE-teNEtbheLs130_assertion type Assertion NP865948.RA4Qe8v95HT5GuSrE0AoZDV1gZnya3LxsE-teNEtbheLs130_head.
- NP865948.RA4Qe8v95HT5GuSrE0AoZDV1gZnya3LxsE-teNEtbheLs130_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." NP865948.RA4Qe8v95HT5GuSrE0AoZDV1gZnya3LxsE-teNEtbheLs130_provenance.
- NP865948.RA4Qe8v95HT5GuSrE0AoZDV1gZnya3LxsE-teNEtbheLs130_assertion evidence source_evidence_literature NP865948.RA4Qe8v95HT5GuSrE0AoZDV1gZnya3LxsE-teNEtbheLs130_provenance.
- NP865948.RA4Qe8v95HT5GuSrE0AoZDV1gZnya3LxsE-teNEtbheLs130_assertion SIO_000772 16849371 NP865948.RA4Qe8v95HT5GuSrE0AoZDV1gZnya3LxsE-teNEtbheLs130_provenance.
- NP865948.RA4Qe8v95HT5GuSrE0AoZDV1gZnya3LxsE-teNEtbheLs130_assertion wasDerivedFrom befree-20140225 NP865948.RA4Qe8v95HT5GuSrE0AoZDV1gZnya3LxsE-teNEtbheLs130_provenance.
- NP865948.RA4Qe8v95HT5GuSrE0AoZDV1gZnya3LxsE-teNEtbheLs130_assertion wasGeneratedBy ECO_0000203 NP865948.RA4Qe8v95HT5GuSrE0AoZDV1gZnya3LxsE-teNEtbheLs130_provenance.