Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP403358.RAnBS_1fKhssQqtbgU8vWDJk5VhqXsUBuVZ1CGUzLI044130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP403358.RAnBS_1fKhssQqtbgU8vWDJk5VhqXsUBuVZ1CGUzLI044130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP403358.RAnBS_1fKhssQqtbgU8vWDJk5VhqXsUBuVZ1CGUzLI044130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP403358.RAnBS_1fKhssQqtbgU8vWDJk5VhqXsUBuVZ1CGUzLI044130_provenance.
- NP403358.RAnBS_1fKhssQqtbgU8vWDJk5VhqXsUBuVZ1CGUzLI044130_assertion description "[Moreover, no correlation is detected between the occurrence of hv3005 deletion and C4A null alleles in lupus patients, suggesting that the effects of these genetic polymorphisms on predisposition to lupus are independent.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP403358.RAnBS_1fKhssQqtbgU8vWDJk5VhqXsUBuVZ1CGUzLI044130_provenance.
- NP403358.RAnBS_1fKhssQqtbgU8vWDJk5VhqXsUBuVZ1CGUzLI044130_assertion evidence source_evidence_literature NP403358.RAnBS_1fKhssQqtbgU8vWDJk5VhqXsUBuVZ1CGUzLI044130_provenance.
- NP403358.RAnBS_1fKhssQqtbgU8vWDJk5VhqXsUBuVZ1CGUzLI044130_assertion SIO_000772 7706484 NP403358.RAnBS_1fKhssQqtbgU8vWDJk5VhqXsUBuVZ1CGUzLI044130_provenance.
- NP403358.RAnBS_1fKhssQqtbgU8vWDJk5VhqXsUBuVZ1CGUzLI044130_assertion wasDerivedFrom befree-20140225 NP403358.RAnBS_1fKhssQqtbgU8vWDJk5VhqXsUBuVZ1CGUzLI044130_provenance.
- NP403358.RAnBS_1fKhssQqtbgU8vWDJk5VhqXsUBuVZ1CGUzLI044130_assertion wasGeneratedBy ECO_0000203 NP403358.RAnBS_1fKhssQqtbgU8vWDJk5VhqXsUBuVZ1CGUzLI044130_provenance.
- befree-20140225 importedOn "2014-02-25" NP403358.RAnBS_1fKhssQqtbgU8vWDJk5VhqXsUBuVZ1CGUzLI044130_provenance.