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- source_evidence_literature type ECO_0000212 NP427469.RAhXq_Lp-JrV_cIowC7q7Q-dJ44k-HOChiNx1lFvI05mI130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP427469.RAhXq_Lp-JrV_cIowC7q7Q-dJ44k-HOChiNx1lFvI05mI130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP427469.RAhXq_Lp-JrV_cIowC7q7Q-dJ44k-HOChiNx1lFvI05mI130_provenance.
- 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.
- befree-20140225 importedOn "2014-02-25" NP427469.RAhXq_Lp-JrV_cIowC7q7Q-dJ44k-HOChiNx1lFvI05mI130_provenance.