Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP417485.RAufwO2qQyYcxplrjOovw09sEZro2Oy1bsjZ9XVzWqr0g130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP417485.RAufwO2qQyYcxplrjOovw09sEZro2Oy1bsjZ9XVzWqr0g130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP417485.RAufwO2qQyYcxplrjOovw09sEZro2Oy1bsjZ9XVzWqr0g130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP417485.RAufwO2qQyYcxplrjOovw09sEZro2Oy1bsjZ9XVzWqr0g130_provenance.
- NP417485.RAufwO2qQyYcxplrjOovw09sEZro2Oy1bsjZ9XVzWqr0g130_assertion description "[A molecular defect in coproporphyrinogen oxidase gene causing harderoporphyria, a variant form of hereditary coproporphyria.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP417485.RAufwO2qQyYcxplrjOovw09sEZro2Oy1bsjZ9XVzWqr0g130_provenance.
- NP417485.RAufwO2qQyYcxplrjOovw09sEZro2Oy1bsjZ9XVzWqr0g130_assertion evidence source_evidence_literature NP417485.RAufwO2qQyYcxplrjOovw09sEZro2Oy1bsjZ9XVzWqr0g130_provenance.
- NP417485.RAufwO2qQyYcxplrjOovw09sEZro2Oy1bsjZ9XVzWqr0g130_assertion SIO_000772 7757079 NP417485.RAufwO2qQyYcxplrjOovw09sEZro2Oy1bsjZ9XVzWqr0g130_provenance.
- NP417485.RAufwO2qQyYcxplrjOovw09sEZro2Oy1bsjZ9XVzWqr0g130_assertion wasDerivedFrom befree-20140225 NP417485.RAufwO2qQyYcxplrjOovw09sEZro2Oy1bsjZ9XVzWqr0g130_provenance.
- NP417485.RAufwO2qQyYcxplrjOovw09sEZro2Oy1bsjZ9XVzWqr0g130_assertion wasGeneratedBy ECO_0000203 NP417485.RAufwO2qQyYcxplrjOovw09sEZro2Oy1bsjZ9XVzWqr0g130_provenance.
- befree-20140225 importedOn "2014-02-25" NP417485.RAufwO2qQyYcxplrjOovw09sEZro2Oy1bsjZ9XVzWqr0g130_provenance.