Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP1319173.RA22KmiUvLnNPqi0jELN0myeyQ6XH2tFgHrlkJPyDjvuQ130_assertion> ?p ?o ?g. }
Showing items 1 to 6 of
6
with 100 items per page.
- NP1319173.RA22KmiUvLnNPqi0jELN0myeyQ6XH2tFgHrlkJPyDjvuQ130_assertion type Assertion NP1319173.RA22KmiUvLnNPqi0jELN0myeyQ6XH2tFgHrlkJPyDjvuQ130_head.
- NP1319173.RA22KmiUvLnNPqi0jELN0myeyQ6XH2tFgHrlkJPyDjvuQ130_assertion description "[Hepatoerythropoietic porphyria is a severe cutaneous porphyria caused by deficiency of uroporphyrinogen decarboxylase and is considered to be the homozygous form of familial (type II) porphyria cutanea tarda.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1319173.RA22KmiUvLnNPqi0jELN0myeyQ6XH2tFgHrlkJPyDjvuQ130_provenance.
- NP1319173.RA22KmiUvLnNPqi0jELN0myeyQ6XH2tFgHrlkJPyDjvuQ130_assertion evidence source_evidence_literature NP1319173.RA22KmiUvLnNPqi0jELN0myeyQ6XH2tFgHrlkJPyDjvuQ130_provenance.
- NP1319173.RA22KmiUvLnNPqi0jELN0myeyQ6XH2tFgHrlkJPyDjvuQ130_assertion SIO_000772 7706766 NP1319173.RA22KmiUvLnNPqi0jELN0myeyQ6XH2tFgHrlkJPyDjvuQ130_provenance.
- NP1319173.RA22KmiUvLnNPqi0jELN0myeyQ6XH2tFgHrlkJPyDjvuQ130_assertion wasDerivedFrom befree-2016 NP1319173.RA22KmiUvLnNPqi0jELN0myeyQ6XH2tFgHrlkJPyDjvuQ130_provenance.
- NP1319173.RA22KmiUvLnNPqi0jELN0myeyQ6XH2tFgHrlkJPyDjvuQ130_assertion wasGeneratedBy ECO_0000203 NP1319173.RA22KmiUvLnNPqi0jELN0myeyQ6XH2tFgHrlkJPyDjvuQ130_provenance.