Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP57370.RAJybxXxv8ZCKS4tySHWJWrO4n3xEA_7WVENOPzngn7n8130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP57370.RAJybxXxv8ZCKS4tySHWJWrO4n3xEA_7WVENOPzngn7n8130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP57370.RAJybxXxv8ZCKS4tySHWJWrO4n3xEA_7WVENOPzngn7n8130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP57370.RAJybxXxv8ZCKS4tySHWJWrO4n3xEA_7WVENOPzngn7n8130_provenance.
- NP57370.RAJybxXxv8ZCKS4tySHWJWrO4n3xEA_7WVENOPzngn7n8130_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 Behcet'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." NP57370.RAJybxXxv8ZCKS4tySHWJWrO4n3xEA_7WVENOPzngn7n8130_provenance.
- NP57370.RAJybxXxv8ZCKS4tySHWJWrO4n3xEA_7WVENOPzngn7n8130_assertion evidence source_evidence_literature NP57370.RAJybxXxv8ZCKS4tySHWJWrO4n3xEA_7WVENOPzngn7n8130_provenance.
- NP57370.RAJybxXxv8ZCKS4tySHWJWrO4n3xEA_7WVENOPzngn7n8130_assertion SIO_000772 14651522 NP57370.RAJybxXxv8ZCKS4tySHWJWrO4n3xEA_7WVENOPzngn7n8130_provenance.
- NP57370.RAJybxXxv8ZCKS4tySHWJWrO4n3xEA_7WVENOPzngn7n8130_assertion wasDerivedFrom gad-20150221 NP57370.RAJybxXxv8ZCKS4tySHWJWrO4n3xEA_7WVENOPzngn7n8130_provenance.
- NP57370.RAJybxXxv8ZCKS4tySHWJWrO4n3xEA_7WVENOPzngn7n8130_assertion wasGeneratedBy ECO_0000203 NP57370.RAJybxXxv8ZCKS4tySHWJWrO4n3xEA_7WVENOPzngn7n8130_provenance.
- gad-20150221 importedOn "2015-02-21" NP57370.RAJybxXxv8ZCKS4tySHWJWrO4n3xEA_7WVENOPzngn7n8130_provenance.