Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP1018146.RASW0342U9ju7vh4O3eK07uP1CdkZC8gldHPzFeumXRaM130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP1018146.RASW0342U9ju7vh4O3eK07uP1CdkZC8gldHPzFeumXRaM130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP1018146.RASW0342U9ju7vh4O3eK07uP1CdkZC8gldHPzFeumXRaM130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP1018146.RASW0342U9ju7vh4O3eK07uP1CdkZC8gldHPzFeumXRaM130_provenance.
- NP1018146.RASW0342U9ju7vh4O3eK07uP1CdkZC8gldHPzFeumXRaM130_assertion description "[Historically, VHL was the only frequently mutated gene in clear cell renal cell carcinoma (ccRCC), with conflicting clinical relevance.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1018146.RASW0342U9ju7vh4O3eK07uP1CdkZC8gldHPzFeumXRaM130_provenance.
- NP1018146.RASW0342U9ju7vh4O3eK07uP1CdkZC8gldHPzFeumXRaM130_assertion evidence source_evidence_literature NP1018146.RASW0342U9ju7vh4O3eK07uP1CdkZC8gldHPzFeumXRaM130_provenance.
- NP1018146.RASW0342U9ju7vh4O3eK07uP1CdkZC8gldHPzFeumXRaM130_assertion SIO_000772 23036577 NP1018146.RASW0342U9ju7vh4O3eK07uP1CdkZC8gldHPzFeumXRaM130_provenance.
- NP1018146.RASW0342U9ju7vh4O3eK07uP1CdkZC8gldHPzFeumXRaM130_assertion wasDerivedFrom befree-2016 NP1018146.RASW0342U9ju7vh4O3eK07uP1CdkZC8gldHPzFeumXRaM130_provenance.
- NP1018146.RASW0342U9ju7vh4O3eK07uP1CdkZC8gldHPzFeumXRaM130_assertion wasGeneratedBy ECO_0000203 NP1018146.RASW0342U9ju7vh4O3eK07uP1CdkZC8gldHPzFeumXRaM130_provenance.
- befree-2016 importedOn "2016-02-19" NP1018146.RASW0342U9ju7vh4O3eK07uP1CdkZC8gldHPzFeumXRaM130_provenance.