Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP924209.RApSnB9X5ZE5wBi6xsFBAdQ8K0XxFWrshIfrH21crTVUs130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP924209.RApSnB9X5ZE5wBi6xsFBAdQ8K0XxFWrshIfrH21crTVUs130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP924209.RApSnB9X5ZE5wBi6xsFBAdQ8K0XxFWrshIfrH21crTVUs130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP924209.RApSnB9X5ZE5wBi6xsFBAdQ8K0XxFWrshIfrH21crTVUs130_provenance.
- NP924209.RApSnB9X5ZE5wBi6xsFBAdQ8K0XxFWrshIfrH21crTVUs130_assertion description "[Clinical assessment of ACG risk is recommended for BEST1 mutation carriers and their first degree relatives.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP924209.RApSnB9X5ZE5wBi6xsFBAdQ8K0XxFWrshIfrH21crTVUs130_provenance.
- NP924209.RApSnB9X5ZE5wBi6xsFBAdQ8K0XxFWrshIfrH21crTVUs130_assertion evidence source_evidence_literature NP924209.RApSnB9X5ZE5wBi6xsFBAdQ8K0XxFWrshIfrH21crTVUs130_provenance.
- NP924209.RApSnB9X5ZE5wBi6xsFBAdQ8K0XxFWrshIfrH21crTVUs130_assertion SIO_000772 21921978 NP924209.RApSnB9X5ZE5wBi6xsFBAdQ8K0XxFWrshIfrH21crTVUs130_provenance.
- NP924209.RApSnB9X5ZE5wBi6xsFBAdQ8K0XxFWrshIfrH21crTVUs130_assertion wasDerivedFrom befree-2016 NP924209.RApSnB9X5ZE5wBi6xsFBAdQ8K0XxFWrshIfrH21crTVUs130_provenance.
- NP924209.RApSnB9X5ZE5wBi6xsFBAdQ8K0XxFWrshIfrH21crTVUs130_assertion wasGeneratedBy ECO_0000203 NP924209.RApSnB9X5ZE5wBi6xsFBAdQ8K0XxFWrshIfrH21crTVUs130_provenance.
- befree-2016 importedOn "2016-02-19" NP924209.RApSnB9X5ZE5wBi6xsFBAdQ8K0XxFWrshIfrH21crTVUs130_provenance.