Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP767240.RAqmHDkSmSW2x9E4Mu4V5ogd-6-qGBBym6TeBl2dLY1CY130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP767240.RAqmHDkSmSW2x9E4Mu4V5ogd-6-qGBBym6TeBl2dLY1CY130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP767240.RAqmHDkSmSW2x9E4Mu4V5ogd-6-qGBBym6TeBl2dLY1CY130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP767240.RAqmHDkSmSW2x9E4Mu4V5ogd-6-qGBBym6TeBl2dLY1CY130_provenance.
- 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.
- befree-20150227 importedOn "2015-02-27" NP767240.RAqmHDkSmSW2x9E4Mu4V5ogd-6-qGBBym6TeBl2dLY1CY130_provenance.