Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP970222.RAczFAahpeDr4Q_MFg92oy9YnNk8n2qsmptcQsxKDPOZM130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP970222.RAczFAahpeDr4Q_MFg92oy9YnNk8n2qsmptcQsxKDPOZM130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP970222.RAczFAahpeDr4Q_MFg92oy9YnNk8n2qsmptcQsxKDPOZM130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP970222.RAczFAahpeDr4Q_MFg92oy9YnNk8n2qsmptcQsxKDPOZM130_provenance.
- NP970222.RAczFAahpeDr4Q_MFg92oy9YnNk8n2qsmptcQsxKDPOZM130_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." NP970222.RAczFAahpeDr4Q_MFg92oy9YnNk8n2qsmptcQsxKDPOZM130_provenance.
- NP970222.RAczFAahpeDr4Q_MFg92oy9YnNk8n2qsmptcQsxKDPOZM130_assertion evidence source_evidence_literature NP970222.RAczFAahpeDr4Q_MFg92oy9YnNk8n2qsmptcQsxKDPOZM130_provenance.
- NP970222.RAczFAahpeDr4Q_MFg92oy9YnNk8n2qsmptcQsxKDPOZM130_assertion SIO_000772 11222331 NP970222.RAczFAahpeDr4Q_MFg92oy9YnNk8n2qsmptcQsxKDPOZM130_provenance.
- NP970222.RAczFAahpeDr4Q_MFg92oy9YnNk8n2qsmptcQsxKDPOZM130_assertion wasDerivedFrom befree-20150227 NP970222.RAczFAahpeDr4Q_MFg92oy9YnNk8n2qsmptcQsxKDPOZM130_provenance.
- NP970222.RAczFAahpeDr4Q_MFg92oy9YnNk8n2qsmptcQsxKDPOZM130_assertion wasGeneratedBy ECO_0000203 NP970222.RAczFAahpeDr4Q_MFg92oy9YnNk8n2qsmptcQsxKDPOZM130_provenance.
- befree-20150227 importedOn "2015-02-27" NP970222.RAczFAahpeDr4Q_MFg92oy9YnNk8n2qsmptcQsxKDPOZM130_provenance.