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- source_evidence_literature type ECO_0000212 NP936419.RAG1bkCw8KXWRB7kfi3fHR7YSz1hr3Fn-FTmNFtfVWK48130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP936419.RAG1bkCw8KXWRB7kfi3fHR7YSz1hr3Fn-FTmNFtfVWK48130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP936419.RAG1bkCw8KXWRB7kfi3fHR7YSz1hr3Fn-FTmNFtfVWK48130_provenance.
- NP936419.RAG1bkCw8KXWRB7kfi3fHR7YSz1hr3Fn-FTmNFtfVWK48130_assertion description "[Hereditary coproporphyria (HC) is an acute hepatic porphyria with autosomal dominant inheritance caused by a deficient activity of coproporphyrinogen IX oxidase (CPX).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP936419.RAG1bkCw8KXWRB7kfi3fHR7YSz1hr3Fn-FTmNFtfVWK48130_provenance.
- NP936419.RAG1bkCw8KXWRB7kfi3fHR7YSz1hr3Fn-FTmNFtfVWK48130_assertion evidence source_evidence_literature NP936419.RAG1bkCw8KXWRB7kfi3fHR7YSz1hr3Fn-FTmNFtfVWK48130_provenance.
- NP936419.RAG1bkCw8KXWRB7kfi3fHR7YSz1hr3Fn-FTmNFtfVWK48130_assertion SIO_000772 7757079 NP936419.RAG1bkCw8KXWRB7kfi3fHR7YSz1hr3Fn-FTmNFtfVWK48130_provenance.
- NP936419.RAG1bkCw8KXWRB7kfi3fHR7YSz1hr3Fn-FTmNFtfVWK48130_assertion wasDerivedFrom befree-20140225 NP936419.RAG1bkCw8KXWRB7kfi3fHR7YSz1hr3Fn-FTmNFtfVWK48130_provenance.
- NP936419.RAG1bkCw8KXWRB7kfi3fHR7YSz1hr3Fn-FTmNFtfVWK48130_assertion wasGeneratedBy ECO_0000203 NP936419.RAG1bkCw8KXWRB7kfi3fHR7YSz1hr3Fn-FTmNFtfVWK48130_provenance.
- befree-20140225 importedOn "2014-02-25" NP936419.RAG1bkCw8KXWRB7kfi3fHR7YSz1hr3Fn-FTmNFtfVWK48130_provenance.