Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP105038.RAcW49syCMOw0FWKjFg0R95OUsiVmzYRt-qYl8lwUQQcU130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP105038.RAcW49syCMOw0FWKjFg0R95OUsiVmzYRt-qYl8lwUQQcU130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP105038.RAcW49syCMOw0FWKjFg0R95OUsiVmzYRt-qYl8lwUQQcU130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP105038.RAcW49syCMOw0FWKjFg0R95OUsiVmzYRt-qYl8lwUQQcU130_provenance.
- NP105038.RAcW49syCMOw0FWKjFg0R95OUsiVmzYRt-qYl8lwUQQcU130_assertion description "[IVS5-275 T>G and Ex10+837 T>C in addition to three tagging SNPs from HapMap database, which provided a comprehensive coverage of genetic variations in the PTGS2 gene in Chinese were genotyped among 257 AD patients and 244 age-matched healthy Chinese subjects.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP105038.RAcW49syCMOw0FWKjFg0R95OUsiVmzYRt-qYl8lwUQQcU130_provenance.
- NP105038.RAcW49syCMOw0FWKjFg0R95OUsiVmzYRt-qYl8lwUQQcU130_assertion evidence source_evidence_literature NP105038.RAcW49syCMOw0FWKjFg0R95OUsiVmzYRt-qYl8lwUQQcU130_provenance.
- NP105038.RAcW49syCMOw0FWKjFg0R95OUsiVmzYRt-qYl8lwUQQcU130_assertion SIO_000772 17234302 NP105038.RAcW49syCMOw0FWKjFg0R95OUsiVmzYRt-qYl8lwUQQcU130_provenance.
- NP105038.RAcW49syCMOw0FWKjFg0R95OUsiVmzYRt-qYl8lwUQQcU130_assertion wasDerivedFrom gad-20150221 NP105038.RAcW49syCMOw0FWKjFg0R95OUsiVmzYRt-qYl8lwUQQcU130_provenance.
- NP105038.RAcW49syCMOw0FWKjFg0R95OUsiVmzYRt-qYl8lwUQQcU130_assertion wasGeneratedBy ECO_0000203 NP105038.RAcW49syCMOw0FWKjFg0R95OUsiVmzYRt-qYl8lwUQQcU130_provenance.
- gad-20150221 importedOn "2015-02-21" NP105038.RAcW49syCMOw0FWKjFg0R95OUsiVmzYRt-qYl8lwUQQcU130_provenance.