Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP701557.RAIMvlFWhh8nR241IU4xkQQnpAopOsZsM81fjNI4shupQ130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP701557.RAIMvlFWhh8nR241IU4xkQQnpAopOsZsM81fjNI4shupQ130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP701557.RAIMvlFWhh8nR241IU4xkQQnpAopOsZsM81fjNI4shupQ130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP701557.RAIMvlFWhh8nR241IU4xkQQnpAopOsZsM81fjNI4shupQ130_provenance.
- NP701557.RAIMvlFWhh8nR241IU4xkQQnpAopOsZsM81fjNI4shupQ130_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." NP701557.RAIMvlFWhh8nR241IU4xkQQnpAopOsZsM81fjNI4shupQ130_provenance.
- NP701557.RAIMvlFWhh8nR241IU4xkQQnpAopOsZsM81fjNI4shupQ130_assertion evidence source_evidence_literature NP701557.RAIMvlFWhh8nR241IU4xkQQnpAopOsZsM81fjNI4shupQ130_provenance.
- NP701557.RAIMvlFWhh8nR241IU4xkQQnpAopOsZsM81fjNI4shupQ130_assertion SIO_000772 9837813 NP701557.RAIMvlFWhh8nR241IU4xkQQnpAopOsZsM81fjNI4shupQ130_provenance.
- NP701557.RAIMvlFWhh8nR241IU4xkQQnpAopOsZsM81fjNI4shupQ130_assertion wasDerivedFrom befree-20140225 NP701557.RAIMvlFWhh8nR241IU4xkQQnpAopOsZsM81fjNI4shupQ130_provenance.
- NP701557.RAIMvlFWhh8nR241IU4xkQQnpAopOsZsM81fjNI4shupQ130_assertion wasGeneratedBy ECO_0000203 NP701557.RAIMvlFWhh8nR241IU4xkQQnpAopOsZsM81fjNI4shupQ130_provenance.
- befree-20140225 importedOn "2014-02-25" NP701557.RAIMvlFWhh8nR241IU4xkQQnpAopOsZsM81fjNI4shupQ130_provenance.