Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP498439.RAyr5q84JzKH4QeXgFuGXV7UbFJ2hQh0FT3cYq3_TWGJA130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP498439.RAyr5q84JzKH4QeXgFuGXV7UbFJ2hQh0FT3cYq3_TWGJA130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP498439.RAyr5q84JzKH4QeXgFuGXV7UbFJ2hQh0FT3cYq3_TWGJA130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP498439.RAyr5q84JzKH4QeXgFuGXV7UbFJ2hQh0FT3cYq3_TWGJA130_provenance.
- NP498439.RAyr5q84JzKH4QeXgFuGXV7UbFJ2hQh0FT3cYq3_TWGJA130_assertion description "[RAD51L1 is a tumor-suppressor gene belonging to the RAD51 family, already implicated in many tumors (uterine leiomyomas, pseudo-Meigs syndromes, pulmonary chondroid hamartomas) and involved in recombinational repair of DNA double-strand breaks.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP498439.RAyr5q84JzKH4QeXgFuGXV7UbFJ2hQh0FT3cYq3_TWGJA130_provenance.
- NP498439.RAyr5q84JzKH4QeXgFuGXV7UbFJ2hQh0FT3cYq3_TWGJA130_assertion evidence source_evidence_literature NP498439.RAyr5q84JzKH4QeXgFuGXV7UbFJ2hQh0FT3cYq3_TWGJA130_provenance.
- NP498439.RAyr5q84JzKH4QeXgFuGXV7UbFJ2hQh0FT3cYq3_TWGJA130_assertion SIO_000772 15942943 NP498439.RAyr5q84JzKH4QeXgFuGXV7UbFJ2hQh0FT3cYq3_TWGJA130_provenance.
- NP498439.RAyr5q84JzKH4QeXgFuGXV7UbFJ2hQh0FT3cYq3_TWGJA130_assertion wasDerivedFrom befree-2016 NP498439.RAyr5q84JzKH4QeXgFuGXV7UbFJ2hQh0FT3cYq3_TWGJA130_provenance.
- NP498439.RAyr5q84JzKH4QeXgFuGXV7UbFJ2hQh0FT3cYq3_TWGJA130_assertion wasGeneratedBy ECO_0000203 NP498439.RAyr5q84JzKH4QeXgFuGXV7UbFJ2hQh0FT3cYq3_TWGJA130_provenance.
- befree-2016 importedOn "2016-02-19" NP498439.RAyr5q84JzKH4QeXgFuGXV7UbFJ2hQh0FT3cYq3_TWGJA130_provenance.