Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP1247513.RAVl1kfi5TFYNjmQy1lUgsvPOttYAT_-GxTpDwtO4qb5Q130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP1247513.RAVl1kfi5TFYNjmQy1lUgsvPOttYAT_-GxTpDwtO4qb5Q130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP1247513.RAVl1kfi5TFYNjmQy1lUgsvPOttYAT_-GxTpDwtO4qb5Q130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP1247513.RAVl1kfi5TFYNjmQy1lUgsvPOttYAT_-GxTpDwtO4qb5Q130_provenance.
- NP1247513.RAVl1kfi5TFYNjmQy1lUgsvPOttYAT_-GxTpDwtO4qb5Q130_assertion description "[Identification of a novel duplication mutation in the VHL gene in a large Chinese family with Von Hippel-Lindau (VHL) syndrome.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1247513.RAVl1kfi5TFYNjmQy1lUgsvPOttYAT_-GxTpDwtO4qb5Q130_provenance.
- NP1247513.RAVl1kfi5TFYNjmQy1lUgsvPOttYAT_-GxTpDwtO4qb5Q130_assertion evidence source_evidence_literature NP1247513.RAVl1kfi5TFYNjmQy1lUgsvPOttYAT_-GxTpDwtO4qb5Q130_provenance.
- NP1247513.RAVl1kfi5TFYNjmQy1lUgsvPOttYAT_-GxTpDwtO4qb5Q130_assertion SIO_000772 25501229 NP1247513.RAVl1kfi5TFYNjmQy1lUgsvPOttYAT_-GxTpDwtO4qb5Q130_provenance.
- NP1247513.RAVl1kfi5TFYNjmQy1lUgsvPOttYAT_-GxTpDwtO4qb5Q130_assertion wasDerivedFrom befree-2016 NP1247513.RAVl1kfi5TFYNjmQy1lUgsvPOttYAT_-GxTpDwtO4qb5Q130_provenance.
- NP1247513.RAVl1kfi5TFYNjmQy1lUgsvPOttYAT_-GxTpDwtO4qb5Q130_assertion wasGeneratedBy ECO_0000203 NP1247513.RAVl1kfi5TFYNjmQy1lUgsvPOttYAT_-GxTpDwtO4qb5Q130_provenance.
- befree-2016 importedOn "2016-02-19" NP1247513.RAVl1kfi5TFYNjmQy1lUgsvPOttYAT_-GxTpDwtO4qb5Q130_provenance.