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- source_evidence_literature type ECO_0000212 NP683987.RAOQn_VfwmXRBcxVe-0_Z-TWH9I1qT47KQ8KU2_d0IzGY130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP683987.RAOQn_VfwmXRBcxVe-0_Z-TWH9I1qT47KQ8KU2_d0IzGY130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP683987.RAOQn_VfwmXRBcxVe-0_Z-TWH9I1qT47KQ8KU2_d0IzGY130_provenance.
- NP683987.RAOQn_VfwmXRBcxVe-0_Z-TWH9I1qT47KQ8KU2_d0IzGY130_assertion description "[We analyzed the frequency of single-nucleotide polymorphisms (SNPs) in genes encoding CCL2 (-2518 and -2076) and CCL5 (-403 and -28) in patients with Beh�et's disease (BD), a systemic form of uveitis, and patients with retinal vasculitis (RV), an organ-specific form of disease.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP683987.RAOQn_VfwmXRBcxVe-0_Z-TWH9I1qT47KQ8KU2_d0IzGY130_provenance.
- NP683987.RAOQn_VfwmXRBcxVe-0_Z-TWH9I1qT47KQ8KU2_d0IzGY130_assertion evidence source_evidence_literature NP683987.RAOQn_VfwmXRBcxVe-0_Z-TWH9I1qT47KQ8KU2_d0IzGY130_provenance.
- NP683987.RAOQn_VfwmXRBcxVe-0_Z-TWH9I1qT47KQ8KU2_d0IzGY130_assertion SIO_000772 14651522 NP683987.RAOQn_VfwmXRBcxVe-0_Z-TWH9I1qT47KQ8KU2_d0IzGY130_provenance.
- NP683987.RAOQn_VfwmXRBcxVe-0_Z-TWH9I1qT47KQ8KU2_d0IzGY130_assertion wasDerivedFrom befree-20150227 NP683987.RAOQn_VfwmXRBcxVe-0_Z-TWH9I1qT47KQ8KU2_d0IzGY130_provenance.
- NP683987.RAOQn_VfwmXRBcxVe-0_Z-TWH9I1qT47KQ8KU2_d0IzGY130_assertion wasGeneratedBy ECO_0000203 NP683987.RAOQn_VfwmXRBcxVe-0_Z-TWH9I1qT47KQ8KU2_d0IzGY130_provenance.
- befree-20150227 importedOn "2015-02-27" NP683987.RAOQn_VfwmXRBcxVe-0_Z-TWH9I1qT47KQ8KU2_d0IzGY130_provenance.