Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP180761.RAF5bxWv8bSi9JusL_6o5vyUW6Fv1KJNRAmUcCrNz3WNE130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP180761.RAF5bxWv8bSi9JusL_6o5vyUW6Fv1KJNRAmUcCrNz3WNE130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP180761.RAF5bxWv8bSi9JusL_6o5vyUW6Fv1KJNRAmUcCrNz3WNE130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP180761.RAF5bxWv8bSi9JusL_6o5vyUW6Fv1KJNRAmUcCrNz3WNE130_provenance.
- NP180761.RAF5bxWv8bSi9JusL_6o5vyUW6Fv1KJNRAmUcCrNz3WNE130_assertion description "[These results suggest that polymorphisms in and haplotypes of the RAD51L1 gene, which is involved in the double-strand break repair pathway, modulate gamma-radiation-induced mutagen sensitivity.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP180761.RAF5bxWv8bSi9JusL_6o5vyUW6Fv1KJNRAmUcCrNz3WNE130_provenance.
- NP180761.RAF5bxWv8bSi9JusL_6o5vyUW6Fv1KJNRAmUcCrNz3WNE130_assertion evidence source_evidence_literature NP180761.RAF5bxWv8bSi9JusL_6o5vyUW6Fv1KJNRAmUcCrNz3WNE130_provenance.
- NP180761.RAF5bxWv8bSi9JusL_6o5vyUW6Fv1KJNRAmUcCrNz3WNE130_assertion SIO_000772 20610542 NP180761.RAF5bxWv8bSi9JusL_6o5vyUW6Fv1KJNRAmUcCrNz3WNE130_provenance.
- NP180761.RAF5bxWv8bSi9JusL_6o5vyUW6Fv1KJNRAmUcCrNz3WNE130_assertion wasDerivedFrom gad-20150221 NP180761.RAF5bxWv8bSi9JusL_6o5vyUW6Fv1KJNRAmUcCrNz3WNE130_provenance.
- NP180761.RAF5bxWv8bSi9JusL_6o5vyUW6Fv1KJNRAmUcCrNz3WNE130_assertion wasGeneratedBy ECO_0000203 NP180761.RAF5bxWv8bSi9JusL_6o5vyUW6Fv1KJNRAmUcCrNz3WNE130_provenance.
- gad-20150221 importedOn "2015-02-21" NP180761.RAF5bxWv8bSi9JusL_6o5vyUW6Fv1KJNRAmUcCrNz3WNE130_provenance.