Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP487464.RAOxyjb_81c5jwRuB3JbtoR7ERYN8-I1ENlz7aTF-UUpg130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP487464.RAOxyjb_81c5jwRuB3JbtoR7ERYN8-I1ENlz7aTF-UUpg130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP487464.RAOxyjb_81c5jwRuB3JbtoR7ERYN8-I1ENlz7aTF-UUpg130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP487464.RAOxyjb_81c5jwRuB3JbtoR7ERYN8-I1ENlz7aTF-UUpg130_provenance.
- befree-2016 importedOn "2016-02-19" NP487464.RAOxyjb_81c5jwRuB3JbtoR7ERYN8-I1ENlz7aTF-UUpg130_provenance.
- NP487464.RAOxyjb_81c5jwRuB3JbtoR7ERYN8-I1ENlz7aTF-UUpg130_assertion wasGeneratedBy ECO_0000203 NP487464.RAOxyjb_81c5jwRuB3JbtoR7ERYN8-I1ENlz7aTF-UUpg130_provenance.
- NP487464.RAOxyjb_81c5jwRuB3JbtoR7ERYN8-I1ENlz7aTF-UUpg130_assertion wasDerivedFrom befree-2016 NP487464.RAOxyjb_81c5jwRuB3JbtoR7ERYN8-I1ENlz7aTF-UUpg130_provenance.
- NP487464.RAOxyjb_81c5jwRuB3JbtoR7ERYN8-I1ENlz7aTF-UUpg130_assertion SIO_000772 15794202 NP487464.RAOxyjb_81c5jwRuB3JbtoR7ERYN8-I1ENlz7aTF-UUpg130_provenance.
- NP487464.RAOxyjb_81c5jwRuB3JbtoR7ERYN8-I1ENlz7aTF-UUpg130_assertion evidence source_evidence_literature NP487464.RAOxyjb_81c5jwRuB3JbtoR7ERYN8-I1ENlz7aTF-UUpg130_provenance.
- NP487464.RAOxyjb_81c5jwRuB3JbtoR7ERYN8-I1ENlz7aTF-UUpg130_assertion description "[To study the frequency of a C4A gene deletions as the genetic basis of C4A protein deficiency (C4AQ0) and its associated haplotypes in Icelandic families with systemic lupus erythematosus (SLE).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP487464.RAOxyjb_81c5jwRuB3JbtoR7ERYN8-I1ENlz7aTF-UUpg130_provenance.