Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP422959.RAHaYAQtpjt49QxtM0aWDEqINgL1f26wPCmdJiESsgl1s130_assertion> ?p ?o ?g. }
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- NP422959.RAHaYAQtpjt49QxtM0aWDEqINgL1f26wPCmdJiESsgl1s130_assertion type Assertion NP422959.RAHaYAQtpjt49QxtM0aWDEqINgL1f26wPCmdJiESsgl1s130_head.
- NP422959.RAHaYAQtpjt49QxtM0aWDEqINgL1f26wPCmdJiESsgl1s130_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." NP422959.RAHaYAQtpjt49QxtM0aWDEqINgL1f26wPCmdJiESsgl1s130_provenance.
- NP422959.RAHaYAQtpjt49QxtM0aWDEqINgL1f26wPCmdJiESsgl1s130_assertion evidence source_evidence_literature NP422959.RAHaYAQtpjt49QxtM0aWDEqINgL1f26wPCmdJiESsgl1s130_provenance.
- NP422959.RAHaYAQtpjt49QxtM0aWDEqINgL1f26wPCmdJiESsgl1s130_assertion SIO_000772 14651522 NP422959.RAHaYAQtpjt49QxtM0aWDEqINgL1f26wPCmdJiESsgl1s130_provenance.
- NP422959.RAHaYAQtpjt49QxtM0aWDEqINgL1f26wPCmdJiESsgl1s130_assertion wasDerivedFrom befree-2016 NP422959.RAHaYAQtpjt49QxtM0aWDEqINgL1f26wPCmdJiESsgl1s130_provenance.
- NP422959.RAHaYAQtpjt49QxtM0aWDEqINgL1f26wPCmdJiESsgl1s130_assertion wasGeneratedBy ECO_0000203 NP422959.RAHaYAQtpjt49QxtM0aWDEqINgL1f26wPCmdJiESsgl1s130_provenance.