Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP427469.RAhXq_Lp-JrV_cIowC7q7Q-dJ44k-HOChiNx1lFvI05mI130_assertion> ?p ?o ?g. }
Showing items 1 to 6 of
6
with 100 items per page.
- NP427469.RAhXq_Lp-JrV_cIowC7q7Q-dJ44k-HOChiNx1lFvI05mI130_assertion type Assertion NP427469.RAhXq_Lp-JrV_cIowC7q7Q-dJ44k-HOChiNx1lFvI05mI130_head.
- NP427469.RAhXq_Lp-JrV_cIowC7q7Q-dJ44k-HOChiNx1lFvI05mI130_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." NP427469.RAhXq_Lp-JrV_cIowC7q7Q-dJ44k-HOChiNx1lFvI05mI130_provenance.
- NP427469.RAhXq_Lp-JrV_cIowC7q7Q-dJ44k-HOChiNx1lFvI05mI130_assertion evidence source_evidence_literature NP427469.RAhXq_Lp-JrV_cIowC7q7Q-dJ44k-HOChiNx1lFvI05mI130_provenance.
- NP427469.RAhXq_Lp-JrV_cIowC7q7Q-dJ44k-HOChiNx1lFvI05mI130_assertion SIO_000772 7706766 NP427469.RAhXq_Lp-JrV_cIowC7q7Q-dJ44k-HOChiNx1lFvI05mI130_provenance.
- NP427469.RAhXq_Lp-JrV_cIowC7q7Q-dJ44k-HOChiNx1lFvI05mI130_assertion wasDerivedFrom befree-20140225 NP427469.RAhXq_Lp-JrV_cIowC7q7Q-dJ44k-HOChiNx1lFvI05mI130_provenance.
- NP427469.RAhXq_Lp-JrV_cIowC7q7Q-dJ44k-HOChiNx1lFvI05mI130_assertion wasGeneratedBy ECO_0000203 NP427469.RAhXq_Lp-JrV_cIowC7q7Q-dJ44k-HOChiNx1lFvI05mI130_provenance.