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- source_evidence_literature type ECO_0000212 NP1246359.RArB2i7em3O1vQoTHOmrefh5p8ncgmcFnQ6hH1IH_5ZSc130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP1246359.RArB2i7em3O1vQoTHOmrefh5p8ncgmcFnQ6hH1IH_5ZSc130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP1246359.RArB2i7em3O1vQoTHOmrefh5p8ncgmcFnQ6hH1IH_5ZSc130_provenance.
- NP1246359.RArB2i7em3O1vQoTHOmrefh5p8ncgmcFnQ6hH1IH_5ZSc130_assertion description "[We also genotyped specific EFHC1 variants in IGE cases and controls from multiple ethnic backgrounds, including 17 African American IGE patients, with 24 matched controls, and 92 Caucasian JME patients with 103 matched controls.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1246359.RArB2i7em3O1vQoTHOmrefh5p8ncgmcFnQ6hH1IH_5ZSc130_provenance.
- NP1246359.RArB2i7em3O1vQoTHOmrefh5p8ncgmcFnQ6hH1IH_5ZSc130_assertion evidence source_evidence_literature NP1246359.RArB2i7em3O1vQoTHOmrefh5p8ncgmcFnQ6hH1IH_5ZSc130_provenance.
- NP1246359.RArB2i7em3O1vQoTHOmrefh5p8ncgmcFnQ6hH1IH_5ZSc130_assertion SIO_000772 25489633 NP1246359.RArB2i7em3O1vQoTHOmrefh5p8ncgmcFnQ6hH1IH_5ZSc130_provenance.
- NP1246359.RArB2i7em3O1vQoTHOmrefh5p8ncgmcFnQ6hH1IH_5ZSc130_assertion wasDerivedFrom befree-2016 NP1246359.RArB2i7em3O1vQoTHOmrefh5p8ncgmcFnQ6hH1IH_5ZSc130_provenance.
- NP1246359.RArB2i7em3O1vQoTHOmrefh5p8ncgmcFnQ6hH1IH_5ZSc130_assertion wasGeneratedBy ECO_0000203 NP1246359.RArB2i7em3O1vQoTHOmrefh5p8ncgmcFnQ6hH1IH_5ZSc130_provenance.
- befree-2016 importedOn "2016-02-19" NP1246359.RArB2i7em3O1vQoTHOmrefh5p8ncgmcFnQ6hH1IH_5ZSc130_provenance.