Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP691375.RA47vJQjO0M6jFNODD1QkukTQdTjcmYjqB8vHMX8iyNr4130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP691375.RA47vJQjO0M6jFNODD1QkukTQdTjcmYjqB8vHMX8iyNr4130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP691375.RA47vJQjO0M6jFNODD1QkukTQdTjcmYjqB8vHMX8iyNr4130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP691375.RA47vJQjO0M6jFNODD1QkukTQdTjcmYjqB8vHMX8iyNr4130_provenance.
- NP691375.RA47vJQjO0M6jFNODD1QkukTQdTjcmYjqB8vHMX8iyNr4130_assertion description "[A RAG1 mutation found in Omenn syndrome causes coding flank hypersensitivity: a novel mechanism for antigen receptor repertoire restriction.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP691375.RA47vJQjO0M6jFNODD1QkukTQdTjcmYjqB8vHMX8iyNr4130_provenance.
- NP691375.RA47vJQjO0M6jFNODD1QkukTQdTjcmYjqB8vHMX8iyNr4130_assertion evidence source_evidence_literature NP691375.RA47vJQjO0M6jFNODD1QkukTQdTjcmYjqB8vHMX8iyNr4130_provenance.
- NP691375.RA47vJQjO0M6jFNODD1QkukTQdTjcmYjqB8vHMX8iyNr4130_assertion SIO_000772 18768869 NP691375.RA47vJQjO0M6jFNODD1QkukTQdTjcmYjqB8vHMX8iyNr4130_provenance.
- NP691375.RA47vJQjO0M6jFNODD1QkukTQdTjcmYjqB8vHMX8iyNr4130_assertion wasDerivedFrom befree-2016 NP691375.RA47vJQjO0M6jFNODD1QkukTQdTjcmYjqB8vHMX8iyNr4130_provenance.
- NP691375.RA47vJQjO0M6jFNODD1QkukTQdTjcmYjqB8vHMX8iyNr4130_assertion wasGeneratedBy ECO_0000203 NP691375.RA47vJQjO0M6jFNODD1QkukTQdTjcmYjqB8vHMX8iyNr4130_provenance.
- befree-2016 importedOn "2016-02-19" NP691375.RA47vJQjO0M6jFNODD1QkukTQdTjcmYjqB8vHMX8iyNr4130_provenance.