Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP137866.RAhR0UxXhIivGJTh9QastunwFIxxLmZNwHM52D51ByaRg130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP137866.RAhR0UxXhIivGJTh9QastunwFIxxLmZNwHM52D51ByaRg130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP137866.RAhR0UxXhIivGJTh9QastunwFIxxLmZNwHM52D51ByaRg130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP137866.RAhR0UxXhIivGJTh9QastunwFIxxLmZNwHM52D51ByaRg130_provenance.
- NP137866.RAhR0UxXhIivGJTh9QastunwFIxxLmZNwHM52D51ByaRg130_assertion description "[Our association findings support the hypothesis that GRM4 sequence variants might confer low-risk effects to the etiology of IGE. A minor pathogenetic contribution of the examined variants is possible. These exploratory findings warrant further replicatio]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP137866.RAhR0UxXhIivGJTh9QastunwFIxxLmZNwHM52D51ByaRg130_provenance.
- NP137866.RAhR0UxXhIivGJTh9QastunwFIxxLmZNwHM52D51ByaRg130_assertion evidence source_evidence_literature NP137866.RAhR0UxXhIivGJTh9QastunwFIxxLmZNwHM52D51ByaRg130_provenance.
- NP137866.RAhR0UxXhIivGJTh9QastunwFIxxLmZNwHM52D51ByaRg130_assertion SIO_000772 20338729 NP137866.RAhR0UxXhIivGJTh9QastunwFIxxLmZNwHM52D51ByaRg130_provenance.
- NP137866.RAhR0UxXhIivGJTh9QastunwFIxxLmZNwHM52D51ByaRg130_assertion wasDerivedFrom gad-20150221 NP137866.RAhR0UxXhIivGJTh9QastunwFIxxLmZNwHM52D51ByaRg130_provenance.
- NP137866.RAhR0UxXhIivGJTh9QastunwFIxxLmZNwHM52D51ByaRg130_assertion wasGeneratedBy ECO_0000203 NP137866.RAhR0UxXhIivGJTh9QastunwFIxxLmZNwHM52D51ByaRg130_provenance.
- gad-20150221 importedOn "2015-02-21" NP137866.RAhR0UxXhIivGJTh9QastunwFIxxLmZNwHM52D51ByaRg130_provenance.