Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP148751.RAfGmF90go7GpCE5r00nx9Pmefg0oIVqZjeCJYKZiIeo8130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP148751.RAfGmF90go7GpCE5r00nx9Pmefg0oIVqZjeCJYKZiIeo8130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP148751.RAfGmF90go7GpCE5r00nx9Pmefg0oIVqZjeCJYKZiIeo8130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP148751.RAfGmF90go7GpCE5r00nx9Pmefg0oIVqZjeCJYKZiIeo8130_provenance.
- NP148751.RAfGmF90go7GpCE5r00nx9Pmefg0oIVqZjeCJYKZiIeo8130_assertion description "[Using a large inception cohort and strict statistical evaluation, we could not identify an association between functional TLR variants and RA phenotype and disease severity. This suggests the functional TLR variants do not play a major role in RA phenotyp]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP148751.RAfGmF90go7GpCE5r00nx9Pmefg0oIVqZjeCJYKZiIeo8130_provenance.
- NP148751.RAfGmF90go7GpCE5r00nx9Pmefg0oIVqZjeCJYKZiIeo8130_assertion evidence source_evidence_literature NP148751.RAfGmF90go7GpCE5r00nx9Pmefg0oIVqZjeCJYKZiIeo8130_provenance.
- NP148751.RAfGmF90go7GpCE5r00nx9Pmefg0oIVqZjeCJYKZiIeo8130_assertion SIO_000772 20194452 NP148751.RAfGmF90go7GpCE5r00nx9Pmefg0oIVqZjeCJYKZiIeo8130_provenance.
- NP148751.RAfGmF90go7GpCE5r00nx9Pmefg0oIVqZjeCJYKZiIeo8130_assertion wasDerivedFrom gad-20150221 NP148751.RAfGmF90go7GpCE5r00nx9Pmefg0oIVqZjeCJYKZiIeo8130_provenance.
- NP148751.RAfGmF90go7GpCE5r00nx9Pmefg0oIVqZjeCJYKZiIeo8130_assertion wasGeneratedBy ECO_0000203 NP148751.RAfGmF90go7GpCE5r00nx9Pmefg0oIVqZjeCJYKZiIeo8130_provenance.
- gad-20150221 importedOn "2015-02-21" NP148751.RAfGmF90go7GpCE5r00nx9Pmefg0oIVqZjeCJYKZiIeo8130_provenance.