Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP74985.RA6GdO-Lgv3P0b97LFYbo923aT5AJL-ot9VWFNQTJiTQs130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP74985.RA6GdO-Lgv3P0b97LFYbo923aT5AJL-ot9VWFNQTJiTQs130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP74985.RA6GdO-Lgv3P0b97LFYbo923aT5AJL-ot9VWFNQTJiTQs130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP74985.RA6GdO-Lgv3P0b97LFYbo923aT5AJL-ot9VWFNQTJiTQs130_provenance.
- NP74985.RA6GdO-Lgv3P0b97LFYbo923aT5AJL-ot9VWFNQTJiTQs130_assertion description "[ Screening of highly prevalent mutations in known genes involved in these disorders does not yield additional relevant information. Differential diagnosis of hereditary autoinflammatory syndromes can be made by thorough clinical examination followed by ta]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP74985.RA6GdO-Lgv3P0b97LFYbo923aT5AJL-ot9VWFNQTJiTQs130_provenance.
- NP74985.RA6GdO-Lgv3P0b97LFYbo923aT5AJL-ot9VWFNQTJiTQs130_assertion evidence source_evidence_literature NP74985.RA6GdO-Lgv3P0b97LFYbo923aT5AJL-ot9VWFNQTJiTQs130_provenance.
- NP74985.RA6GdO-Lgv3P0b97LFYbo923aT5AJL-ot9VWFNQTJiTQs130_assertion SIO_000772 16234278 NP74985.RA6GdO-Lgv3P0b97LFYbo923aT5AJL-ot9VWFNQTJiTQs130_provenance.
- NP74985.RA6GdO-Lgv3P0b97LFYbo923aT5AJL-ot9VWFNQTJiTQs130_assertion wasDerivedFrom gad-20150221 NP74985.RA6GdO-Lgv3P0b97LFYbo923aT5AJL-ot9VWFNQTJiTQs130_provenance.
- NP74985.RA6GdO-Lgv3P0b97LFYbo923aT5AJL-ot9VWFNQTJiTQs130_assertion wasGeneratedBy ECO_0000203 NP74985.RA6GdO-Lgv3P0b97LFYbo923aT5AJL-ot9VWFNQTJiTQs130_provenance.
- gad-20150221 importedOn "2015-02-21" NP74985.RA6GdO-Lgv3P0b97LFYbo923aT5AJL-ot9VWFNQTJiTQs130_provenance.