Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP422814.RAikF5WJksPVbYqo-FW3y1UyJXAsK5E7_bd4coc7X9KWM130_assertion> ?p ?o ?g. }
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- NP422814.RAikF5WJksPVbYqo-FW3y1UyJXAsK5E7_bd4coc7X9KWM130_assertion type Assertion NP422814.RAikF5WJksPVbYqo-FW3y1UyJXAsK5E7_bd4coc7X9KWM130_head.
- 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.
- NP422814.RAikF5WJksPVbYqo-FW3y1UyJXAsK5E7_bd4coc7X9KWM130_assertion evidence source_evidence_literature NP422814.RAikF5WJksPVbYqo-FW3y1UyJXAsK5E7_bd4coc7X9KWM130_provenance.
- NP422814.RAikF5WJksPVbYqo-FW3y1UyJXAsK5E7_bd4coc7X9KWM130_assertion SIO_000772 7757079 NP422814.RAikF5WJksPVbYqo-FW3y1UyJXAsK5E7_bd4coc7X9KWM130_provenance.
- NP422814.RAikF5WJksPVbYqo-FW3y1UyJXAsK5E7_bd4coc7X9KWM130_assertion wasDerivedFrom befree-20140225 NP422814.RAikF5WJksPVbYqo-FW3y1UyJXAsK5E7_bd4coc7X9KWM130_provenance.
- NP422814.RAikF5WJksPVbYqo-FW3y1UyJXAsK5E7_bd4coc7X9KWM130_assertion wasGeneratedBy ECO_0000203 NP422814.RAikF5WJksPVbYqo-FW3y1UyJXAsK5E7_bd4coc7X9KWM130_provenance.