Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP161839.RAzCnlBMn8G7cYgCvN_Wkd93yC4SVCmxwun2U9I1rMWcc130_assertion> ?p ?o ?g. }
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- NP161839.RAzCnlBMn8G7cYgCvN_Wkd93yC4SVCmxwun2U9I1rMWcc130_assertion type Assertion NP161839.RAzCnlBMn8G7cYgCvN_Wkd93yC4SVCmxwun2U9I1rMWcc130_head.
- NP161839.RAzCnlBMn8G7cYgCvN_Wkd93yC4SVCmxwun2U9I1rMWcc130_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." NP161839.RAzCnlBMn8G7cYgCvN_Wkd93yC4SVCmxwun2U9I1rMWcc130_provenance.
- NP161839.RAzCnlBMn8G7cYgCvN_Wkd93yC4SVCmxwun2U9I1rMWcc130_assertion evidence source_evidence_literature NP161839.RAzCnlBMn8G7cYgCvN_Wkd93yC4SVCmxwun2U9I1rMWcc130_provenance.
- NP161839.RAzCnlBMn8G7cYgCvN_Wkd93yC4SVCmxwun2U9I1rMWcc130_assertion SIO_000772 7706766 NP161839.RAzCnlBMn8G7cYgCvN_Wkd93yC4SVCmxwun2U9I1rMWcc130_provenance.
- NP161839.RAzCnlBMn8G7cYgCvN_Wkd93yC4SVCmxwun2U9I1rMWcc130_assertion wasDerivedFrom befree-20140225 NP161839.RAzCnlBMn8G7cYgCvN_Wkd93yC4SVCmxwun2U9I1rMWcc130_provenance.
- NP161839.RAzCnlBMn8G7cYgCvN_Wkd93yC4SVCmxwun2U9I1rMWcc130_assertion wasGeneratedBy ECO_0000203 NP161839.RAzCnlBMn8G7cYgCvN_Wkd93yC4SVCmxwun2U9I1rMWcc130_provenance.