Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP66782.RAWhp42qW6LWM9JM3LwogwH7hgp4w9-dw52WdA44qlaxE130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP66782.RAWhp42qW6LWM9JM3LwogwH7hgp4w9-dw52WdA44qlaxE130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP66782.RAWhp42qW6LWM9JM3LwogwH7hgp4w9-dw52WdA44qlaxE130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP66782.RAWhp42qW6LWM9JM3LwogwH7hgp4w9-dw52WdA44qlaxE130_provenance.
- NP66782.RAWhp42qW6LWM9JM3LwogwH7hgp4w9-dw52WdA44qlaxE130_assertion description "[HLA-DQA1*0201-DQB1*0201 haplotype is involved in susceptibility, conferring 5.53 times more risk of developing this disease. EBM rating: B-2b.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP66782.RAWhp42qW6LWM9JM3LwogwH7hgp4w9-dw52WdA44qlaxE130_provenance.
- NP66782.RAWhp42qW6LWM9JM3LwogwH7hgp4w9-dw52WdA44qlaxE130_assertion evidence source_evidence_literature NP66782.RAWhp42qW6LWM9JM3LwogwH7hgp4w9-dw52WdA44qlaxE130_provenance.
- NP66782.RAWhp42qW6LWM9JM3LwogwH7hgp4w9-dw52WdA44qlaxE130_assertion SIO_000772 16890076 NP66782.RAWhp42qW6LWM9JM3LwogwH7hgp4w9-dw52WdA44qlaxE130_provenance.
- NP66782.RAWhp42qW6LWM9JM3LwogwH7hgp4w9-dw52WdA44qlaxE130_assertion wasDerivedFrom gad-20130706 NP66782.RAWhp42qW6LWM9JM3LwogwH7hgp4w9-dw52WdA44qlaxE130_provenance.
- NP66782.RAWhp42qW6LWM9JM3LwogwH7hgp4w9-dw52WdA44qlaxE130_assertion wasGeneratedBy ECO_0000203 NP66782.RAWhp42qW6LWM9JM3LwogwH7hgp4w9-dw52WdA44qlaxE130_provenance.
- gad-20130706 importedOn "2013-07-06" NP66782.RAWhp42qW6LWM9JM3LwogwH7hgp4w9-dw52WdA44qlaxE130_provenance.