Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP50807.RADVKi7Ljje_-NGp3fS6dH_umjj9dAg-jmjESYlEsIEhc130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP50807.RADVKi7Ljje_-NGp3fS6dH_umjj9dAg-jmjESYlEsIEhc130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP50807.RADVKi7Ljje_-NGp3fS6dH_umjj9dAg-jmjESYlEsIEhc130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP50807.RADVKi7Ljje_-NGp3fS6dH_umjj9dAg-jmjESYlEsIEhc130_provenance.
- NP50807.RADVKi7Ljje_-NGp3fS6dH_umjj9dAg-jmjESYlEsIEhc130_assertion description "[The rare C allele frequency of TBXA2R+795T>C was significantly higher in AIA than in ATA (P=0.03) and the TBXA2R+795T>C polymorphism was also associated with extent of percent fall in forced expiratory volume in 1 s (FEV1) after the inhalation of lysine-acetyl salicylic acid in AIA patients (P=0.009); AIA patients homozygous for the +795 C allele had a greater percent fall of FEV1 compared with individuals with TBXA2R+795 CT or TT genotypes.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP50807.RADVKi7Ljje_-NGp3fS6dH_umjj9dAg-jmjESYlEsIEhc130_provenance.
- NP50807.RADVKi7Ljje_-NGp3fS6dH_umjj9dAg-jmjESYlEsIEhc130_assertion evidence source_evidence_literature NP50807.RADVKi7Ljje_-NGp3fS6dH_umjj9dAg-jmjESYlEsIEhc130_provenance.
- NP50807.RADVKi7Ljje_-NGp3fS6dH_umjj9dAg-jmjESYlEsIEhc130_assertion SIO_000772 15898979 NP50807.RADVKi7Ljje_-NGp3fS6dH_umjj9dAg-jmjESYlEsIEhc130_provenance.
- NP50807.RADVKi7Ljje_-NGp3fS6dH_umjj9dAg-jmjESYlEsIEhc130_assertion wasDerivedFrom gad-20130706 NP50807.RADVKi7Ljje_-NGp3fS6dH_umjj9dAg-jmjESYlEsIEhc130_provenance.
- NP50807.RADVKi7Ljje_-NGp3fS6dH_umjj9dAg-jmjESYlEsIEhc130_assertion wasGeneratedBy ECO_0000203 NP50807.RADVKi7Ljje_-NGp3fS6dH_umjj9dAg-jmjESYlEsIEhc130_provenance.
- gad-20130706 importedOn "2013-07-06" NP50807.RADVKi7Ljje_-NGp3fS6dH_umjj9dAg-jmjESYlEsIEhc130_provenance.