Matches in Nanopublications for { ?s ?p "[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."@en ?g. }
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- NP422814.RAikF5WJksPVbYqo-FW3y1UyJXAsK5E7_bd4coc7X9KWM130_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." NP422814.RAikF5WJksPVbYqo-FW3y1UyJXAsK5E7_bd4coc7X9KWM130_provenance.
- NP524997.RAyJIGt5OpmVRKWpZegJ5IKzajrGYpNuky9XPJqWxP3ZM130_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." NP524997.RAyJIGt5OpmVRKWpZegJ5IKzajrGYpNuky9XPJqWxP3ZM130_provenance.
- NP695546.RAzWPv9LtvSn8jXtQtHAITMJvMSAOrenMGRUXlRDSw9uI130_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." NP695546.RAzWPv9LtvSn8jXtQtHAITMJvMSAOrenMGRUXlRDSw9uI130_provenance.
- NP781285.RAzl4teoQ_uemi9OFh7IgOC9EC3K9R9zkVLpZ0MFwS45g130_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." NP781285.RAzl4teoQ_uemi9OFh7IgOC9EC3K9R9zkVLpZ0MFwS45g130_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.