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- source_evidence_literature type ECO_0000212 NP1410091.RAnB4GZm3Hq27Zqsx8YpP4HBV5UJTGGvhebMe66DnP-Bw130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP1410091.RAnB4GZm3Hq27Zqsx8YpP4HBV5UJTGGvhebMe66DnP-Bw130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP1410091.RAnB4GZm3Hq27Zqsx8YpP4HBV5UJTGGvhebMe66DnP-Bw130_provenance.
- NP1410091.RAnB4GZm3Hq27Zqsx8YpP4HBV5UJTGGvhebMe66DnP-Bw130_assertion description "[Sequence analysis of SURF-1 revealed mutations in numerous DNA samples from LD(COX-) patients, indicating that this gene is responsible for the major complementation group in this important mitochondrial disorder.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1410091.RAnB4GZm3Hq27Zqsx8YpP4HBV5UJTGGvhebMe66DnP-Bw130_provenance.
- NP1410091.RAnB4GZm3Hq27Zqsx8YpP4HBV5UJTGGvhebMe66DnP-Bw130_assertion evidence source_evidence_literature NP1410091.RAnB4GZm3Hq27Zqsx8YpP4HBV5UJTGGvhebMe66DnP-Bw130_provenance.
- NP1410091.RAnB4GZm3Hq27Zqsx8YpP4HBV5UJTGGvhebMe66DnP-Bw130_assertion SIO_000772 9837813 NP1410091.RAnB4GZm3Hq27Zqsx8YpP4HBV5UJTGGvhebMe66DnP-Bw130_provenance.
- NP1410091.RAnB4GZm3Hq27Zqsx8YpP4HBV5UJTGGvhebMe66DnP-Bw130_assertion wasDerivedFrom befree-2016 NP1410091.RAnB4GZm3Hq27Zqsx8YpP4HBV5UJTGGvhebMe66DnP-Bw130_provenance.
- NP1410091.RAnB4GZm3Hq27Zqsx8YpP4HBV5UJTGGvhebMe66DnP-Bw130_assertion wasGeneratedBy ECO_0000203 NP1410091.RAnB4GZm3Hq27Zqsx8YpP4HBV5UJTGGvhebMe66DnP-Bw130_provenance.
- befree-2016 importedOn "2016-02-19" NP1410091.RAnB4GZm3Hq27Zqsx8YpP4HBV5UJTGGvhebMe66DnP-Bw130_provenance.