Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP927436.RACi1M-LgmtfC0jCmfAN0BiD4qfGMz8g7syQPXk99d3FQ130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP927436.RACi1M-LgmtfC0jCmfAN0BiD4qfGMz8g7syQPXk99d3FQ130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP927436.RACi1M-LgmtfC0jCmfAN0BiD4qfGMz8g7syQPXk99d3FQ130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP927436.RACi1M-LgmtfC0jCmfAN0BiD4qfGMz8g7syQPXk99d3FQ130_provenance.
- NP927436.RACi1M-LgmtfC0jCmfAN0BiD4qfGMz8g7syQPXk99d3FQ130_assertion description "[STAT4 polymorphism in a Chinese Han population with Vogt-Koyanagi-Harada syndrome and Beh�et's disease.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP927436.RACi1M-LgmtfC0jCmfAN0BiD4qfGMz8g7syQPXk99d3FQ130_provenance.
- NP927436.RACi1M-LgmtfC0jCmfAN0BiD4qfGMz8g7syQPXk99d3FQ130_assertion evidence source_evidence_literature NP927436.RACi1M-LgmtfC0jCmfAN0BiD4qfGMz8g7syQPXk99d3FQ130_provenance.
- NP927436.RACi1M-LgmtfC0jCmfAN0BiD4qfGMz8g7syQPXk99d3FQ130_assertion SIO_000772 20438790 NP927436.RACi1M-LgmtfC0jCmfAN0BiD4qfGMz8g7syQPXk99d3FQ130_provenance.
- NP927436.RACi1M-LgmtfC0jCmfAN0BiD4qfGMz8g7syQPXk99d3FQ130_assertion wasDerivedFrom befree-20140225 NP927436.RACi1M-LgmtfC0jCmfAN0BiD4qfGMz8g7syQPXk99d3FQ130_provenance.
- NP927436.RACi1M-LgmtfC0jCmfAN0BiD4qfGMz8g7syQPXk99d3FQ130_assertion wasGeneratedBy ECO_0000203 NP927436.RACi1M-LgmtfC0jCmfAN0BiD4qfGMz8g7syQPXk99d3FQ130_provenance.
- befree-20140225 importedOn "2014-02-25" NP927436.RACi1M-LgmtfC0jCmfAN0BiD4qfGMz8g7syQPXk99d3FQ130_provenance.