Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP468580.RATPd_OKpZf5qVEE_wW94XP-BqCFd1TsTAvxnv8XhVeYM130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP468580.RATPd_OKpZf5qVEE_wW94XP-BqCFd1TsTAvxnv8XhVeYM130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP468580.RATPd_OKpZf5qVEE_wW94XP-BqCFd1TsTAvxnv8XhVeYM130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP468580.RATPd_OKpZf5qVEE_wW94XP-BqCFd1TsTAvxnv8XhVeYM130_provenance.
- NP468580.RATPd_OKpZf5qVEE_wW94XP-BqCFd1TsTAvxnv8XhVeYM130_assertion description "[We also observed weak constitutive fragility of the RNU1 and RNU2 loci in cells belonging to xeroderma pigmentosum complementation groups B and D (XPB and XPD) which are partially defective in the ERCC2 (XPD) and ERCC3 (XPB) helicase activities shared between the repairosome and the RNA polymerase H basal transcription factor TFIIH.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP468580.RATPd_OKpZf5qVEE_wW94XP-BqCFd1TsTAvxnv8XhVeYM130_provenance.
- NP468580.RATPd_OKpZf5qVEE_wW94XP-BqCFd1TsTAvxnv8XhVeYM130_assertion evidence source_evidence_literature NP468580.RATPd_OKpZf5qVEE_wW94XP-BqCFd1TsTAvxnv8XhVeYM130_provenance.
- NP468580.RATPd_OKpZf5qVEE_wW94XP-BqCFd1TsTAvxnv8XhVeYM130_assertion SIO_000772 9557707 NP468580.RATPd_OKpZf5qVEE_wW94XP-BqCFd1TsTAvxnv8XhVeYM130_provenance.
- NP468580.RATPd_OKpZf5qVEE_wW94XP-BqCFd1TsTAvxnv8XhVeYM130_assertion wasDerivedFrom befree-20140225 NP468580.RATPd_OKpZf5qVEE_wW94XP-BqCFd1TsTAvxnv8XhVeYM130_provenance.
- NP468580.RATPd_OKpZf5qVEE_wW94XP-BqCFd1TsTAvxnv8XhVeYM130_assertion wasGeneratedBy ECO_0000203 NP468580.RATPd_OKpZf5qVEE_wW94XP-BqCFd1TsTAvxnv8XhVeYM130_provenance.
- befree-20140225 importedOn "2014-02-25" NP468580.RATPd_OKpZf5qVEE_wW94XP-BqCFd1TsTAvxnv8XhVeYM130_provenance.