Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP501391.RAUQ1eqPUqRtPlf7ac96TrT9kUKrTuyc2igM17jQC5vhM130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP501391.RAUQ1eqPUqRtPlf7ac96TrT9kUKrTuyc2igM17jQC5vhM130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP501391.RAUQ1eqPUqRtPlf7ac96TrT9kUKrTuyc2igM17jQC5vhM130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP501391.RAUQ1eqPUqRtPlf7ac96TrT9kUKrTuyc2igM17jQC5vhM130_provenance.
- NP501391.RAUQ1eqPUqRtPlf7ac96TrT9kUKrTuyc2igM17jQC5vhM130_assertion wasGeneratedBy ECO_0000203 NP501391.RAUQ1eqPUqRtPlf7ac96TrT9kUKrTuyc2igM17jQC5vhM130_provenance.
- NP501391.RAUQ1eqPUqRtPlf7ac96TrT9kUKrTuyc2igM17jQC5vhM130_assertion wasDerivedFrom befree-20140225 NP501391.RAUQ1eqPUqRtPlf7ac96TrT9kUKrTuyc2igM17jQC5vhM130_provenance.
- NP501391.RAUQ1eqPUqRtPlf7ac96TrT9kUKrTuyc2igM17jQC5vhM130_assertion SIO_000772 19442274 NP501391.RAUQ1eqPUqRtPlf7ac96TrT9kUKrTuyc2igM17jQC5vhM130_provenance.
- NP501391.RAUQ1eqPUqRtPlf7ac96TrT9kUKrTuyc2igM17jQC5vhM130_assertion evidence source_evidence_literature NP501391.RAUQ1eqPUqRtPlf7ac96TrT9kUKrTuyc2igM17jQC5vhM130_provenance.
- NP501391.RAUQ1eqPUqRtPlf7ac96TrT9kUKrTuyc2igM17jQC5vhM130_assertion description "[Among the associated SNPs, the Behçet's disease-risk allele in rs2061634 leads to substitution of serine to cysteine at amino acid position 995 (S995C) in the KIAA1529 protein.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP501391.RAUQ1eqPUqRtPlf7ac96TrT9kUKrTuyc2igM17jQC5vhM130_provenance.
- befree-20140225 importedOn "2014-02-25" NP501391.RAUQ1eqPUqRtPlf7ac96TrT9kUKrTuyc2igM17jQC5vhM130_provenance.