Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP1307606.RASqyCT2wY4v9hvqRALkh4CNw4ne8lD8QBzRfxXwrcFQk130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP1307606.RASqyCT2wY4v9hvqRALkh4CNw4ne8lD8QBzRfxXwrcFQk130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP1307606.RASqyCT2wY4v9hvqRALkh4CNw4ne8lD8QBzRfxXwrcFQk130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP1307606.RASqyCT2wY4v9hvqRALkh4CNw4ne8lD8QBzRfxXwrcFQk130_provenance.
- NP1307606.RASqyCT2wY4v9hvqRALkh4CNw4ne8lD8QBzRfxXwrcFQk130_assertion description "[Variegate porphyria (VP) is an autosomal dominant disease characterized in adults by mechanical fragility and blistering of sun-exposed skin or acute visceral and neurological manifestations.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1307606.RASqyCT2wY4v9hvqRALkh4CNw4ne8lD8QBzRfxXwrcFQk130_provenance.
- NP1307606.RASqyCT2wY4v9hvqRALkh4CNw4ne8lD8QBzRfxXwrcFQk130_assertion evidence source_evidence_literature NP1307606.RASqyCT2wY4v9hvqRALkh4CNw4ne8lD8QBzRfxXwrcFQk130_provenance.
- NP1307606.RASqyCT2wY4v9hvqRALkh4CNw4ne8lD8QBzRfxXwrcFQk130_assertion SIO_000772 7077804 NP1307606.RASqyCT2wY4v9hvqRALkh4CNw4ne8lD8QBzRfxXwrcFQk130_provenance.
- NP1307606.RASqyCT2wY4v9hvqRALkh4CNw4ne8lD8QBzRfxXwrcFQk130_assertion wasDerivedFrom befree-2016 NP1307606.RASqyCT2wY4v9hvqRALkh4CNw4ne8lD8QBzRfxXwrcFQk130_provenance.
- NP1307606.RASqyCT2wY4v9hvqRALkh4CNw4ne8lD8QBzRfxXwrcFQk130_assertion wasGeneratedBy ECO_0000203 NP1307606.RASqyCT2wY4v9hvqRALkh4CNw4ne8lD8QBzRfxXwrcFQk130_provenance.
- befree-2016 importedOn "2016-02-19" NP1307606.RASqyCT2wY4v9hvqRALkh4CNw4ne8lD8QBzRfxXwrcFQk130_provenance.