Matches in Nanopublications for { ?s ?p "[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."@en ?g. }
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- NP615177.RA4z76mX4ekJFJ6Q3DDaWwb4bn6ixX58PCzT-C_fYUYz8130_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." NP615177.RA4z76mX4ekJFJ6Q3DDaWwb4bn6ixX58PCzT-C_fYUYz8130_provenance.
- 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." provenance.
- NP477042.RACD1YAvUXgDuZeThClOMOhz8FayIDBmEKHSrlb5m0UFE130_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." NP477042.RACD1YAvUXgDuZeThClOMOhz8FayIDBmEKHSrlb5m0UFE130_provenance.
- 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.