Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP822480.RApg30dsiHkKtZbAhLimZRuTPL8n9BxbCJ8spIiLmR6ZM130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP822480.RApg30dsiHkKtZbAhLimZRuTPL8n9BxbCJ8spIiLmR6ZM130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP822480.RApg30dsiHkKtZbAhLimZRuTPL8n9BxbCJ8spIiLmR6ZM130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP822480.RApg30dsiHkKtZbAhLimZRuTPL8n9BxbCJ8spIiLmR6ZM130_provenance.
- NP822480.RApg30dsiHkKtZbAhLimZRuTPL8n9BxbCJ8spIiLmR6ZM130_assertion description "[Bi-allelic germline mutations of the Fanconi anemia (FA) genes, PALB2/FANCN and BRCA2/FANCD1, have been reported in a few Wilms tumor (WT) patients with an atypical FA phenotype.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP822480.RApg30dsiHkKtZbAhLimZRuTPL8n9BxbCJ8spIiLmR6ZM130_provenance.
- NP822480.RApg30dsiHkKtZbAhLimZRuTPL8n9BxbCJ8spIiLmR6ZM130_assertion evidence source_evidence_literature NP822480.RApg30dsiHkKtZbAhLimZRuTPL8n9BxbCJ8spIiLmR6ZM130_provenance.
- NP822480.RApg30dsiHkKtZbAhLimZRuTPL8n9BxbCJ8spIiLmR6ZM130_assertion SIO_000772 20589654 NP822480.RApg30dsiHkKtZbAhLimZRuTPL8n9BxbCJ8spIiLmR6ZM130_provenance.
- NP822480.RApg30dsiHkKtZbAhLimZRuTPL8n9BxbCJ8spIiLmR6ZM130_assertion wasDerivedFrom befree-2016 NP822480.RApg30dsiHkKtZbAhLimZRuTPL8n9BxbCJ8spIiLmR6ZM130_provenance.
- NP822480.RApg30dsiHkKtZbAhLimZRuTPL8n9BxbCJ8spIiLmR6ZM130_assertion wasGeneratedBy ECO_0000203 NP822480.RApg30dsiHkKtZbAhLimZRuTPL8n9BxbCJ8spIiLmR6ZM130_provenance.
- befree-2016 importedOn "2016-02-19" NP822480.RApg30dsiHkKtZbAhLimZRuTPL8n9BxbCJ8spIiLmR6ZM130_provenance.