Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP783827.RAmuRrBtWlsepEaXACENa3JazvE2-VGlQsBEsjWr5urwQ130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP783827.RAmuRrBtWlsepEaXACENa3JazvE2-VGlQsBEsjWr5urwQ130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP783827.RAmuRrBtWlsepEaXACENa3JazvE2-VGlQsBEsjWr5urwQ130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP783827.RAmuRrBtWlsepEaXACENa3JazvE2-VGlQsBEsjWr5urwQ130_provenance.
- NP783827.RAmuRrBtWlsepEaXACENa3JazvE2-VGlQsBEsjWr5urwQ130_assertion description "[These data provide evidence for a regulatory defect in the proteasome system in human autoimmune disorders, pointing to a unique role for LMP2 (beta1i) in the pathogenesis of primary Sj�gren's syndrome.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP783827.RAmuRrBtWlsepEaXACENa3JazvE2-VGlQsBEsjWr5urwQ130_provenance.
- NP783827.RAmuRrBtWlsepEaXACENa3JazvE2-VGlQsBEsjWr5urwQ130_assertion evidence source_evidence_literature NP783827.RAmuRrBtWlsepEaXACENa3JazvE2-VGlQsBEsjWr5urwQ130_provenance.
- NP783827.RAmuRrBtWlsepEaXACENa3JazvE2-VGlQsBEsjWr5urwQ130_assertion SIO_000772 16414974 NP783827.RAmuRrBtWlsepEaXACENa3JazvE2-VGlQsBEsjWr5urwQ130_provenance.
- NP783827.RAmuRrBtWlsepEaXACENa3JazvE2-VGlQsBEsjWr5urwQ130_assertion wasDerivedFrom befree-20140225 NP783827.RAmuRrBtWlsepEaXACENa3JazvE2-VGlQsBEsjWr5urwQ130_provenance.
- NP783827.RAmuRrBtWlsepEaXACENa3JazvE2-VGlQsBEsjWr5urwQ130_assertion wasGeneratedBy ECO_0000203 NP783827.RAmuRrBtWlsepEaXACENa3JazvE2-VGlQsBEsjWr5urwQ130_provenance.
- befree-20140225 importedOn "2014-02-25" NP783827.RAmuRrBtWlsepEaXACENa3JazvE2-VGlQsBEsjWr5urwQ130_provenance.