Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP309278.RAsvewxgc2mi9QbU8K0Z2eB_y8LZBqW3YkWVVzPLdfMJA130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP309278.RAsvewxgc2mi9QbU8K0Z2eB_y8LZBqW3YkWVVzPLdfMJA130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP309278.RAsvewxgc2mi9QbU8K0Z2eB_y8LZBqW3YkWVVzPLdfMJA130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP309278.RAsvewxgc2mi9QbU8K0Z2eB_y8LZBqW3YkWVVzPLdfMJA130_provenance.
- NP309278.RAsvewxgc2mi9QbU8K0Z2eB_y8LZBqW3YkWVVzPLdfMJA130_assertion description "[The DRB1*04-DQA1*03 haplotype is a marker of increased SO susceptibility and severity, as in Vogt-Koyanagi-Harada disease, which also has similar clinicopathological and HLA associations.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP309278.RAsvewxgc2mi9QbU8K0Z2eB_y8LZBqW3YkWVVzPLdfMJA130_provenance.
- NP309278.RAsvewxgc2mi9QbU8K0Z2eB_y8LZBqW3YkWVVzPLdfMJA130_assertion evidence source_evidence_literature NP309278.RAsvewxgc2mi9QbU8K0Z2eB_y8LZBqW3YkWVVzPLdfMJA130_provenance.
- NP309278.RAsvewxgc2mi9QbU8K0Z2eB_y8LZBqW3YkWVVzPLdfMJA130_assertion SIO_000772 11222331 NP309278.RAsvewxgc2mi9QbU8K0Z2eB_y8LZBqW3YkWVVzPLdfMJA130_provenance.
- NP309278.RAsvewxgc2mi9QbU8K0Z2eB_y8LZBqW3YkWVVzPLdfMJA130_assertion wasDerivedFrom befree-2016 NP309278.RAsvewxgc2mi9QbU8K0Z2eB_y8LZBqW3YkWVVzPLdfMJA130_provenance.
- NP309278.RAsvewxgc2mi9QbU8K0Z2eB_y8LZBqW3YkWVVzPLdfMJA130_assertion wasGeneratedBy ECO_0000203 NP309278.RAsvewxgc2mi9QbU8K0Z2eB_y8LZBqW3YkWVVzPLdfMJA130_provenance.
- befree-2016 importedOn "2016-02-19" NP309278.RAsvewxgc2mi9QbU8K0Z2eB_y8LZBqW3YkWVVzPLdfMJA130_provenance.