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- source_evidence_literature type ECO_0000212 NP147402.RAsJWJdD6jMR7Rax-bU01DvrQerl66BSQSk9M2DWEWGNA130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP147402.RAsJWJdD6jMR7Rax-bU01DvrQerl66BSQSk9M2DWEWGNA130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP147402.RAsJWJdD6jMR7Rax-bU01DvrQerl66BSQSk9M2DWEWGNA130_provenance.
- NP147402.RAsJWJdD6jMR7Rax-bU01DvrQerl66BSQSk9M2DWEWGNA130_assertion description "[We identified genetic associations between Behcet's disease and single-nucleotide polymorphisms (SNPs) in KIAA1529, CPVL, LOC100129342, UBASH3B, and UBAC2 (odds ratio = 2.04, 2.26, 1.84, 1.71, and 1.61, respectively; P value = 4.2 x 10-5, 1.0 x 10-4, 3.0 x 10-4, 1.5 x 10-3, and 5.8 x 10-3, respectively).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP147402.RAsJWJdD6jMR7Rax-bU01DvrQerl66BSQSk9M2DWEWGNA130_provenance.
- NP147402.RAsJWJdD6jMR7Rax-bU01DvrQerl66BSQSk9M2DWEWGNA130_assertion evidence source_evidence_literature NP147402.RAsJWJdD6jMR7Rax-bU01DvrQerl66BSQSk9M2DWEWGNA130_provenance.
- NP147402.RAsJWJdD6jMR7Rax-bU01DvrQerl66BSQSk9M2DWEWGNA130_assertion SIO_000772 19442274 NP147402.RAsJWJdD6jMR7Rax-bU01DvrQerl66BSQSk9M2DWEWGNA130_provenance.
- NP147402.RAsJWJdD6jMR7Rax-bU01DvrQerl66BSQSk9M2DWEWGNA130_assertion wasDerivedFrom gad-20150221 NP147402.RAsJWJdD6jMR7Rax-bU01DvrQerl66BSQSk9M2DWEWGNA130_provenance.
- NP147402.RAsJWJdD6jMR7Rax-bU01DvrQerl66BSQSk9M2DWEWGNA130_assertion wasGeneratedBy ECO_0000203 NP147402.RAsJWJdD6jMR7Rax-bU01DvrQerl66BSQSk9M2DWEWGNA130_provenance.
- gad-20150221 importedOn "2015-02-21" NP147402.RAsJWJdD6jMR7Rax-bU01DvrQerl66BSQSk9M2DWEWGNA130_provenance.