Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP477042.RACD1YAvUXgDuZeThClOMOhz8FayIDBmEKHSrlb5m0UFE130_assertion> ?p ?o ?g. }
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- NP477042.RACD1YAvUXgDuZeThClOMOhz8FayIDBmEKHSrlb5m0UFE130_assertion type Assertion NP477042.RACD1YAvUXgDuZeThClOMOhz8FayIDBmEKHSrlb5m0UFE130_head.
- 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.
- NP477042.RACD1YAvUXgDuZeThClOMOhz8FayIDBmEKHSrlb5m0UFE130_assertion evidence source_evidence_literature NP477042.RACD1YAvUXgDuZeThClOMOhz8FayIDBmEKHSrlb5m0UFE130_provenance.
- NP477042.RACD1YAvUXgDuZeThClOMOhz8FayIDBmEKHSrlb5m0UFE130_assertion SIO_000772 15660919 NP477042.RACD1YAvUXgDuZeThClOMOhz8FayIDBmEKHSrlb5m0UFE130_provenance.
- NP477042.RACD1YAvUXgDuZeThClOMOhz8FayIDBmEKHSrlb5m0UFE130_assertion wasDerivedFrom befree-2016 NP477042.RACD1YAvUXgDuZeThClOMOhz8FayIDBmEKHSrlb5m0UFE130_provenance.
- NP477042.RACD1YAvUXgDuZeThClOMOhz8FayIDBmEKHSrlb5m0UFE130_assertion wasGeneratedBy ECO_0000203 NP477042.RACD1YAvUXgDuZeThClOMOhz8FayIDBmEKHSrlb5m0UFE130_provenance.