Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP831819.RAQZisbjK1FTxQvCUU9itizkh45ZxkR9VvzarG6_sK3Ik130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP831819.RAQZisbjK1FTxQvCUU9itizkh45ZxkR9VvzarG6_sK3Ik130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP831819.RAQZisbjK1FTxQvCUU9itizkh45ZxkR9VvzarG6_sK3Ik130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP831819.RAQZisbjK1FTxQvCUU9itizkh45ZxkR9VvzarG6_sK3Ik130_provenance.
- befree-2016 importedOn "2016-02-19" NP831819.RAQZisbjK1FTxQvCUU9itizkh45ZxkR9VvzarG6_sK3Ik130_provenance.
- NP831819.RAQZisbjK1FTxQvCUU9itizkh45ZxkR9VvzarG6_sK3Ik130_assertion wasGeneratedBy ECO_0000203 NP831819.RAQZisbjK1FTxQvCUU9itizkh45ZxkR9VvzarG6_sK3Ik130_provenance.
- NP831819.RAQZisbjK1FTxQvCUU9itizkh45ZxkR9VvzarG6_sK3Ik130_assertion wasDerivedFrom befree-2016 NP831819.RAQZisbjK1FTxQvCUU9itizkh45ZxkR9VvzarG6_sK3Ik130_provenance.
- NP831819.RAQZisbjK1FTxQvCUU9itizkh45ZxkR9VvzarG6_sK3Ik130_assertion SIO_000772 20697805 NP831819.RAQZisbjK1FTxQvCUU9itizkh45ZxkR9VvzarG6_sK3Ik130_provenance.
- NP831819.RAQZisbjK1FTxQvCUU9itizkh45ZxkR9VvzarG6_sK3Ik130_assertion evidence source_evidence_literature NP831819.RAQZisbjK1FTxQvCUU9itizkh45ZxkR9VvzarG6_sK3Ik130_provenance.
- NP831819.RAQZisbjK1FTxQvCUU9itizkh45ZxkR9VvzarG6_sK3Ik130_assertion description "[It has been reported that one biallelic missense mutation in the RAD51C gene was found in a Fanconi anemia-like disorder and six monoallelic pathogenic mutations were identified in 480 BRCA1/2 negative breast and ovarian cancer pedigrees but not in 620 pedigrees with breast cancer only.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP831819.RAQZisbjK1FTxQvCUU9itizkh45ZxkR9VvzarG6_sK3Ik130_provenance.