Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP1410091.RAnB4GZm3Hq27Zqsx8YpP4HBV5UJTGGvhebMe66DnP-Bw130_assertion> ?p ?o ?g. }
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- NP1410091.RAnB4GZm3Hq27Zqsx8YpP4HBV5UJTGGvhebMe66DnP-Bw130_assertion type Assertion NP1410091.RAnB4GZm3Hq27Zqsx8YpP4HBV5UJTGGvhebMe66DnP-Bw130_head.
- 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.