Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP767240.RAqmHDkSmSW2x9E4Mu4V5ogd-6-qGBBym6TeBl2dLY1CY130_assertion> ?p ?o ?g. }
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- NP767240.RAqmHDkSmSW2x9E4Mu4V5ogd-6-qGBBym6TeBl2dLY1CY130_assertion type Assertion NP767240.RAqmHDkSmSW2x9E4Mu4V5ogd-6-qGBBym6TeBl2dLY1CY130_head.
- NP767240.RAqmHDkSmSW2x9E4Mu4V5ogd-6-qGBBym6TeBl2dLY1CY130_assertion description "[Hepatoerythropoietic porphyria (HEP) is an inherited metabolic disorder characterized by the accumulation of porphyrins resulting from a deficiency in uroporphyrinogen decarboxylase (UROD).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP767240.RAqmHDkSmSW2x9E4Mu4V5ogd-6-qGBBym6TeBl2dLY1CY130_provenance.
- NP767240.RAqmHDkSmSW2x9E4Mu4V5ogd-6-qGBBym6TeBl2dLY1CY130_assertion evidence source_evidence_literature NP767240.RAqmHDkSmSW2x9E4Mu4V5ogd-6-qGBBym6TeBl2dLY1CY130_provenance.
- NP767240.RAqmHDkSmSW2x9E4Mu4V5ogd-6-qGBBym6TeBl2dLY1CY130_assertion SIO_000772 10397714 NP767240.RAqmHDkSmSW2x9E4Mu4V5ogd-6-qGBBym6TeBl2dLY1CY130_provenance.
- NP767240.RAqmHDkSmSW2x9E4Mu4V5ogd-6-qGBBym6TeBl2dLY1CY130_assertion wasDerivedFrom befree-20150227 NP767240.RAqmHDkSmSW2x9E4Mu4V5ogd-6-qGBBym6TeBl2dLY1CY130_provenance.
- NP767240.RAqmHDkSmSW2x9E4Mu4V5ogd-6-qGBBym6TeBl2dLY1CY130_assertion wasGeneratedBy ECO_0000203 NP767240.RAqmHDkSmSW2x9E4Mu4V5ogd-6-qGBBym6TeBl2dLY1CY130_provenance.