Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP663632.RAfWGX0pWRYVLLxLV2Hx_jp2AWDtlea1CY3A7iek8VrKk130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP663632.RAfWGX0pWRYVLLxLV2Hx_jp2AWDtlea1CY3A7iek8VrKk130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP663632.RAfWGX0pWRYVLLxLV2Hx_jp2AWDtlea1CY3A7iek8VrKk130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP663632.RAfWGX0pWRYVLLxLV2Hx_jp2AWDtlea1CY3A7iek8VrKk130_provenance.
- NP663632.RAfWGX0pWRYVLLxLV2Hx_jp2AWDtlea1CY3A7iek8VrKk130_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." NP663632.RAfWGX0pWRYVLLxLV2Hx_jp2AWDtlea1CY3A7iek8VrKk130_provenance.
- NP663632.RAfWGX0pWRYVLLxLV2Hx_jp2AWDtlea1CY3A7iek8VrKk130_assertion evidence source_evidence_literature NP663632.RAfWGX0pWRYVLLxLV2Hx_jp2AWDtlea1CY3A7iek8VrKk130_provenance.
- NP663632.RAfWGX0pWRYVLLxLV2Hx_jp2AWDtlea1CY3A7iek8VrKk130_assertion SIO_000772 15942943 NP663632.RAfWGX0pWRYVLLxLV2Hx_jp2AWDtlea1CY3A7iek8VrKk130_provenance.
- NP663632.RAfWGX0pWRYVLLxLV2Hx_jp2AWDtlea1CY3A7iek8VrKk130_assertion wasDerivedFrom befree-20150227 NP663632.RAfWGX0pWRYVLLxLV2Hx_jp2AWDtlea1CY3A7iek8VrKk130_provenance.
- NP663632.RAfWGX0pWRYVLLxLV2Hx_jp2AWDtlea1CY3A7iek8VrKk130_assertion wasGeneratedBy ECO_0000203 NP663632.RAfWGX0pWRYVLLxLV2Hx_jp2AWDtlea1CY3A7iek8VrKk130_provenance.
- befree-20150227 importedOn "2015-02-27" NP663632.RAfWGX0pWRYVLLxLV2Hx_jp2AWDtlea1CY3A7iek8VrKk130_provenance.