Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP179959.RAFePOdufPwAdR-0ulJDvc__NFFHlkU5yoHcX-rgdhHLg130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP179959.RAFePOdufPwAdR-0ulJDvc__NFFHlkU5yoHcX-rgdhHLg130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP179959.RAFePOdufPwAdR-0ulJDvc__NFFHlkU5yoHcX-rgdhHLg130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP179959.RAFePOdufPwAdR-0ulJDvc__NFFHlkU5yoHcX-rgdhHLg130_provenance.
- NP179959.RAFePOdufPwAdR-0ulJDvc__NFFHlkU5yoHcX-rgdhHLg130_assertion description "[After genotyping 120 SNPs of the PTGER gene family for the 1(st) cohort study, four SNPs in PTGER1, ten in PTGER3, six in PTGER3, and a haplotype of PTGER2 showed association signals with decreased or increased risk of AIA.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP179959.RAFePOdufPwAdR-0ulJDvc__NFFHlkU5yoHcX-rgdhHLg130_provenance.
- NP179959.RAFePOdufPwAdR-0ulJDvc__NFFHlkU5yoHcX-rgdhHLg130_assertion evidence source_evidence_literature NP179959.RAFePOdufPwAdR-0ulJDvc__NFFHlkU5yoHcX-rgdhHLg130_provenance.
- NP179959.RAFePOdufPwAdR-0ulJDvc__NFFHlkU5yoHcX-rgdhHLg130_assertion SIO_000772 20587336 NP179959.RAFePOdufPwAdR-0ulJDvc__NFFHlkU5yoHcX-rgdhHLg130_provenance.
- NP179959.RAFePOdufPwAdR-0ulJDvc__NFFHlkU5yoHcX-rgdhHLg130_assertion wasDerivedFrom gad-20150221 NP179959.RAFePOdufPwAdR-0ulJDvc__NFFHlkU5yoHcX-rgdhHLg130_provenance.
- NP179959.RAFePOdufPwAdR-0ulJDvc__NFFHlkU5yoHcX-rgdhHLg130_assertion wasGeneratedBy ECO_0000203 NP179959.RAFePOdufPwAdR-0ulJDvc__NFFHlkU5yoHcX-rgdhHLg130_provenance.
- gad-20150221 importedOn "2015-02-21" NP179959.RAFePOdufPwAdR-0ulJDvc__NFFHlkU5yoHcX-rgdhHLg130_provenance.