Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP551754.RArJfHhVvYxkwd_2ESAyHGrR7PoLI3fzR0kBnFfK4VD2U130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP551754.RArJfHhVvYxkwd_2ESAyHGrR7PoLI3fzR0kBnFfK4VD2U130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP551754.RArJfHhVvYxkwd_2ESAyHGrR7PoLI3fzR0kBnFfK4VD2U130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP551754.RArJfHhVvYxkwd_2ESAyHGrR7PoLI3fzR0kBnFfK4VD2U130_provenance.
- NP551754.RArJfHhVvYxkwd_2ESAyHGrR7PoLI3fzR0kBnFfK4VD2U130_assertion description "[The comparison between LL patients with and without ENL also showed a statistically significant difference in the presence of C4B*Q0, indicating that C4B deficiency itself is associated with ENL.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP551754.RArJfHhVvYxkwd_2ESAyHGrR7PoLI3fzR0kBnFfK4VD2U130_provenance.
- NP551754.RArJfHhVvYxkwd_2ESAyHGrR7PoLI3fzR0kBnFfK4VD2U130_assertion evidence source_evidence_literature NP551754.RArJfHhVvYxkwd_2ESAyHGrR7PoLI3fzR0kBnFfK4VD2U130_provenance.
- NP551754.RArJfHhVvYxkwd_2ESAyHGrR7PoLI3fzR0kBnFfK4VD2U130_assertion SIO_000772 8485914 NP551754.RArJfHhVvYxkwd_2ESAyHGrR7PoLI3fzR0kBnFfK4VD2U130_provenance.
- NP551754.RArJfHhVvYxkwd_2ESAyHGrR7PoLI3fzR0kBnFfK4VD2U130_assertion wasDerivedFrom befree-20140225 NP551754.RArJfHhVvYxkwd_2ESAyHGrR7PoLI3fzR0kBnFfK4VD2U130_provenance.
- NP551754.RArJfHhVvYxkwd_2ESAyHGrR7PoLI3fzR0kBnFfK4VD2U130_assertion wasGeneratedBy ECO_0000203 NP551754.RArJfHhVvYxkwd_2ESAyHGrR7PoLI3fzR0kBnFfK4VD2U130_provenance.
- befree-20140225 importedOn "2014-02-25" NP551754.RArJfHhVvYxkwd_2ESAyHGrR7PoLI3fzR0kBnFfK4VD2U130_provenance.