Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP638489.RA7u6U8911GaRygtCNcFSpmzJPGtF06JohK5MY8M_Bsew130_assertion> ?p ?o ?g. }
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- NP638489.RA7u6U8911GaRygtCNcFSpmzJPGtF06JohK5MY8M_Bsew130_assertion type Assertion NP638489.RA7u6U8911GaRygtCNcFSpmzJPGtF06JohK5MY8M_Bsew130_head.
- NP638489.RA7u6U8911GaRygtCNcFSpmzJPGtF06JohK5MY8M_Bsew130_assertion description "[Overrepresentation of the founder PPOX gene mutation R59W in a South African patient with severe clinical manifestation of porphyria.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP638489.RA7u6U8911GaRygtCNcFSpmzJPGtF06JohK5MY8M_Bsew130_provenance.
- NP638489.RA7u6U8911GaRygtCNcFSpmzJPGtF06JohK5MY8M_Bsew130_assertion evidence source_evidence_literature NP638489.RA7u6U8911GaRygtCNcFSpmzJPGtF06JohK5MY8M_Bsew130_provenance.
- NP638489.RA7u6U8911GaRygtCNcFSpmzJPGtF06JohK5MY8M_Bsew130_assertion SIO_000772 15660919 NP638489.RA7u6U8911GaRygtCNcFSpmzJPGtF06JohK5MY8M_Bsew130_provenance.
- NP638489.RA7u6U8911GaRygtCNcFSpmzJPGtF06JohK5MY8M_Bsew130_assertion wasDerivedFrom befree-20150227 NP638489.RA7u6U8911GaRygtCNcFSpmzJPGtF06JohK5MY8M_Bsew130_provenance.
- NP638489.RA7u6U8911GaRygtCNcFSpmzJPGtF06JohK5MY8M_Bsew130_assertion wasGeneratedBy ECO_0000203 NP638489.RA7u6U8911GaRygtCNcFSpmzJPGtF06JohK5MY8M_Bsew130_provenance.