Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP760033.RAA8ihBrk2ax7LXvAI25ljCx1yJbmYR_WP_eJ4FzvzR8M130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP760033.RAA8ihBrk2ax7LXvAI25ljCx1yJbmYR_WP_eJ4FzvzR8M130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP760033.RAA8ihBrk2ax7LXvAI25ljCx1yJbmYR_WP_eJ4FzvzR8M130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP760033.RAA8ihBrk2ax7LXvAI25ljCx1yJbmYR_WP_eJ4FzvzR8M130_provenance.
- NP760033.RAA8ihBrk2ax7LXvAI25ljCx1yJbmYR_WP_eJ4FzvzR8M130_assertion description "[The DRB1*01 allele was expressed with a frequency of 20.69% in the controls whereas it was only detected in 3.96% of the NPC patients.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP760033.RAA8ihBrk2ax7LXvAI25ljCx1yJbmYR_WP_eJ4FzvzR8M130_provenance.
- NP760033.RAA8ihBrk2ax7LXvAI25ljCx1yJbmYR_WP_eJ4FzvzR8M130_assertion evidence source_evidence_literature NP760033.RAA8ihBrk2ax7LXvAI25ljCx1yJbmYR_WP_eJ4FzvzR8M130_provenance.
- NP760033.RAA8ihBrk2ax7LXvAI25ljCx1yJbmYR_WP_eJ4FzvzR8M130_assertion SIO_000772 19714482 NP760033.RAA8ihBrk2ax7LXvAI25ljCx1yJbmYR_WP_eJ4FzvzR8M130_provenance.
- NP760033.RAA8ihBrk2ax7LXvAI25ljCx1yJbmYR_WP_eJ4FzvzR8M130_assertion wasDerivedFrom befree-2016 NP760033.RAA8ihBrk2ax7LXvAI25ljCx1yJbmYR_WP_eJ4FzvzR8M130_provenance.
- NP760033.RAA8ihBrk2ax7LXvAI25ljCx1yJbmYR_WP_eJ4FzvzR8M130_assertion wasGeneratedBy ECO_0000203 NP760033.RAA8ihBrk2ax7LXvAI25ljCx1yJbmYR_WP_eJ4FzvzR8M130_provenance.
- befree-2016 importedOn "2016-02-19" NP760033.RAA8ihBrk2ax7LXvAI25ljCx1yJbmYR_WP_eJ4FzvzR8M130_provenance.