Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP167097.RAU6K4jmbUL82Rrg8Ag4g1U0W1ntCFfFLtUP8UpgVlFWg130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP167097.RAU6K4jmbUL82Rrg8Ag4g1U0W1ntCFfFLtUP8UpgVlFWg130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP167097.RAU6K4jmbUL82Rrg8Ag4g1U0W1ntCFfFLtUP8UpgVlFWg130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP167097.RAU6K4jmbUL82Rrg8Ag4g1U0W1ntCFfFLtUP8UpgVlFWg130_provenance.
- NP167097.RAU6K4jmbUL82Rrg8Ag4g1U0W1ntCFfFLtUP8UpgVlFWg130_assertion description "[In 62 of 105 patients with proven ARVD/C, mutations were found: 58 in the gene encoding Plakophilin2 (PKP2), 3 in Desmoglein2, 3 in Desmocollin2, and 1 in Desmoplakin.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP167097.RAU6K4jmbUL82Rrg8Ag4g1U0W1ntCFfFLtUP8UpgVlFWg130_provenance.
- NP167097.RAU6K4jmbUL82Rrg8Ag4g1U0W1ntCFfFLtUP8UpgVlFWg130_assertion evidence source_evidence_literature NP167097.RAU6K4jmbUL82Rrg8Ag4g1U0W1ntCFfFLtUP8UpgVlFWg130_provenance.
- NP167097.RAU6K4jmbUL82Rrg8Ag4g1U0W1ntCFfFLtUP8UpgVlFWg130_assertion SIO_000772 20215590 NP167097.RAU6K4jmbUL82Rrg8Ag4g1U0W1ntCFfFLtUP8UpgVlFWg130_provenance.
- NP167097.RAU6K4jmbUL82Rrg8Ag4g1U0W1ntCFfFLtUP8UpgVlFWg130_assertion wasDerivedFrom gad-20150221 NP167097.RAU6K4jmbUL82Rrg8Ag4g1U0W1ntCFfFLtUP8UpgVlFWg130_provenance.
- NP167097.RAU6K4jmbUL82Rrg8Ag4g1U0W1ntCFfFLtUP8UpgVlFWg130_assertion wasGeneratedBy ECO_0000203 NP167097.RAU6K4jmbUL82Rrg8Ag4g1U0W1ntCFfFLtUP8UpgVlFWg130_provenance.
- gad-20150221 importedOn "2015-02-21" NP167097.RAU6K4jmbUL82Rrg8Ag4g1U0W1ntCFfFLtUP8UpgVlFWg130_provenance.