Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP346155.RA3WIuHnpUsgy4ml9mrJgRD3hf8PqPHtlNhSddg0JGoKc130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP346155.RA3WIuHnpUsgy4ml9mrJgRD3hf8PqPHtlNhSddg0JGoKc130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP346155.RA3WIuHnpUsgy4ml9mrJgRD3hf8PqPHtlNhSddg0JGoKc130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP346155.RA3WIuHnpUsgy4ml9mrJgRD3hf8PqPHtlNhSddg0JGoKc130_provenance.
- befree-2016 importedOn "2016-02-19" NP346155.RA3WIuHnpUsgy4ml9mrJgRD3hf8PqPHtlNhSddg0JGoKc130_provenance.
- NP346155.RA3WIuHnpUsgy4ml9mrJgRD3hf8PqPHtlNhSddg0JGoKc130_assertion wasGeneratedBy ECO_0000203 NP346155.RA3WIuHnpUsgy4ml9mrJgRD3hf8PqPHtlNhSddg0JGoKc130_provenance.
- NP346155.RA3WIuHnpUsgy4ml9mrJgRD3hf8PqPHtlNhSddg0JGoKc130_assertion wasDerivedFrom befree-2016 NP346155.RA3WIuHnpUsgy4ml9mrJgRD3hf8PqPHtlNhSddg0JGoKc130_provenance.
- NP346155.RA3WIuHnpUsgy4ml9mrJgRD3hf8PqPHtlNhSddg0JGoKc130_assertion SIO_000772 11857753 NP346155.RA3WIuHnpUsgy4ml9mrJgRD3hf8PqPHtlNhSddg0JGoKc130_provenance.
- NP346155.RA3WIuHnpUsgy4ml9mrJgRD3hf8PqPHtlNhSddg0JGoKc130_assertion evidence source_evidence_literature NP346155.RA3WIuHnpUsgy4ml9mrJgRD3hf8PqPHtlNhSddg0JGoKc130_provenance.
- NP346155.RA3WIuHnpUsgy4ml9mrJgRD3hf8PqPHtlNhSddg0JGoKc130_assertion description "[Co-existence of frataxin and cardiac troponin T gene mutations in a child with Friedreich Ataxia and familial hypertrophic cardiomyopathy.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP346155.RA3WIuHnpUsgy4ml9mrJgRD3hf8PqPHtlNhSddg0JGoKc130_provenance.