Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP828982.RAVIJ8s5lN0NZ-tHnPQNVZonCkiZoK9Lcrh7W-1IhqRPA130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP828982.RAVIJ8s5lN0NZ-tHnPQNVZonCkiZoK9Lcrh7W-1IhqRPA130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP828982.RAVIJ8s5lN0NZ-tHnPQNVZonCkiZoK9Lcrh7W-1IhqRPA130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP828982.RAVIJ8s5lN0NZ-tHnPQNVZonCkiZoK9Lcrh7W-1IhqRPA130_provenance.
- NP828982.RAVIJ8s5lN0NZ-tHnPQNVZonCkiZoK9Lcrh7W-1IhqRPA130_assertion description "[The frequency of patients carrying both the TBXA2R+795T>C rare allele and HLA DPB1(*)0301 was significantly higher in AIA patients (29.4%) than in ATA patients (7.3%) (P=0.008, odds ratio=5.3).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP828982.RAVIJ8s5lN0NZ-tHnPQNVZonCkiZoK9Lcrh7W-1IhqRPA130_provenance.
- NP828982.RAVIJ8s5lN0NZ-tHnPQNVZonCkiZoK9Lcrh7W-1IhqRPA130_assertion evidence source_evidence_literature NP828982.RAVIJ8s5lN0NZ-tHnPQNVZonCkiZoK9Lcrh7W-1IhqRPA130_provenance.
- NP828982.RAVIJ8s5lN0NZ-tHnPQNVZonCkiZoK9Lcrh7W-1IhqRPA130_assertion SIO_000772 15898979 NP828982.RAVIJ8s5lN0NZ-tHnPQNVZonCkiZoK9Lcrh7W-1IhqRPA130_provenance.
- NP828982.RAVIJ8s5lN0NZ-tHnPQNVZonCkiZoK9Lcrh7W-1IhqRPA130_assertion wasDerivedFrom befree-20140225 NP828982.RAVIJ8s5lN0NZ-tHnPQNVZonCkiZoK9Lcrh7W-1IhqRPA130_provenance.
- NP828982.RAVIJ8s5lN0NZ-tHnPQNVZonCkiZoK9Lcrh7W-1IhqRPA130_assertion wasGeneratedBy ECO_0000203 NP828982.RAVIJ8s5lN0NZ-tHnPQNVZonCkiZoK9Lcrh7W-1IhqRPA130_provenance.
- befree-20140225 importedOn "2014-02-25" NP828982.RAVIJ8s5lN0NZ-tHnPQNVZonCkiZoK9Lcrh7W-1IhqRPA130_provenance.