Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP735478.RA0i9Hbv6Gi5faYE-Rrj52C4gEOlJgCEiZu6cTEKznWMw130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP735478.RA0i9Hbv6Gi5faYE-Rrj52C4gEOlJgCEiZu6cTEKznWMw130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP735478.RA0i9Hbv6Gi5faYE-Rrj52C4gEOlJgCEiZu6cTEKznWMw130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP735478.RA0i9Hbv6Gi5faYE-Rrj52C4gEOlJgCEiZu6cTEKznWMw130_provenance.
- NP735478.RA0i9Hbv6Gi5faYE-Rrj52C4gEOlJgCEiZu6cTEKznWMw130_assertion description "[Genetic predisposition to clear cell RCC (CCRCC) is a major feature of von Hippel-Lindau (VHL) disease (MIM 193300) and has rarely been associated with chromosome 3 translocations.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP735478.RA0i9Hbv6Gi5faYE-Rrj52C4gEOlJgCEiZu6cTEKznWMw130_provenance.
- NP735478.RA0i9Hbv6Gi5faYE-Rrj52C4gEOlJgCEiZu6cTEKznWMw130_assertion evidence source_evidence_literature NP735478.RA0i9Hbv6Gi5faYE-Rrj52C4gEOlJgCEiZu6cTEKznWMw130_provenance.
- NP735478.RA0i9Hbv6Gi5faYE-Rrj52C4gEOlJgCEiZu6cTEKznWMw130_assertion SIO_000772 10807693 NP735478.RA0i9Hbv6Gi5faYE-Rrj52C4gEOlJgCEiZu6cTEKznWMw130_provenance.
- NP735478.RA0i9Hbv6Gi5faYE-Rrj52C4gEOlJgCEiZu6cTEKznWMw130_assertion wasDerivedFrom befree-20140225 NP735478.RA0i9Hbv6Gi5faYE-Rrj52C4gEOlJgCEiZu6cTEKznWMw130_provenance.
- NP735478.RA0i9Hbv6Gi5faYE-Rrj52C4gEOlJgCEiZu6cTEKznWMw130_assertion wasGeneratedBy ECO_0000203 NP735478.RA0i9Hbv6Gi5faYE-Rrj52C4gEOlJgCEiZu6cTEKznWMw130_provenance.
- befree-20140225 importedOn "2014-02-25" NP735478.RA0i9Hbv6Gi5faYE-Rrj52C4gEOlJgCEiZu6cTEKznWMw130_provenance.