Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP695546.RAzWPv9LtvSn8jXtQtHAITMJvMSAOrenMGRUXlRDSw9uI130_assertion> ?p ?o ?g. }
Showing items 1 to 6 of
6
with 100 items per page.
- NP695546.RAzWPv9LtvSn8jXtQtHAITMJvMSAOrenMGRUXlRDSw9uI130_assertion type Assertion NP695546.RAzWPv9LtvSn8jXtQtHAITMJvMSAOrenMGRUXlRDSw9uI130_head.
- 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.
- NP695546.RAzWPv9LtvSn8jXtQtHAITMJvMSAOrenMGRUXlRDSw9uI130_assertion evidence source_evidence_literature NP695546.RAzWPv9LtvSn8jXtQtHAITMJvMSAOrenMGRUXlRDSw9uI130_provenance.
- NP695546.RAzWPv9LtvSn8jXtQtHAITMJvMSAOrenMGRUXlRDSw9uI130_assertion SIO_000772 7757079 NP695546.RAzWPv9LtvSn8jXtQtHAITMJvMSAOrenMGRUXlRDSw9uI130_provenance.
- NP695546.RAzWPv9LtvSn8jXtQtHAITMJvMSAOrenMGRUXlRDSw9uI130_assertion wasDerivedFrom befree-20140225 NP695546.RAzWPv9LtvSn8jXtQtHAITMJvMSAOrenMGRUXlRDSw9uI130_provenance.
- NP695546.RAzWPv9LtvSn8jXtQtHAITMJvMSAOrenMGRUXlRDSw9uI130_assertion wasGeneratedBy ECO_0000203 NP695546.RAzWPv9LtvSn8jXtQtHAITMJvMSAOrenMGRUXlRDSw9uI130_provenance.