Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP180783.RALKmlSK6Df6L_e2yFLDOR8kCZATLnnfQNcpyvSh-eneQ130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP180783.RALKmlSK6Df6L_e2yFLDOR8kCZATLnnfQNcpyvSh-eneQ130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP180783.RALKmlSK6Df6L_e2yFLDOR8kCZATLnnfQNcpyvSh-eneQ130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP180783.RALKmlSK6Df6L_e2yFLDOR8kCZATLnnfQNcpyvSh-eneQ130_provenance.
- NP180783.RALKmlSK6Df6L_e2yFLDOR8kCZATLnnfQNcpyvSh-eneQ130_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." NP180783.RALKmlSK6Df6L_e2yFLDOR8kCZATLnnfQNcpyvSh-eneQ130_provenance.
- NP180783.RALKmlSK6Df6L_e2yFLDOR8kCZATLnnfQNcpyvSh-eneQ130_assertion evidence source_evidence_literature NP180783.RALKmlSK6Df6L_e2yFLDOR8kCZATLnnfQNcpyvSh-eneQ130_provenance.
- NP180783.RALKmlSK6Df6L_e2yFLDOR8kCZATLnnfQNcpyvSh-eneQ130_assertion SIO_000772 20610542 NP180783.RALKmlSK6Df6L_e2yFLDOR8kCZATLnnfQNcpyvSh-eneQ130_provenance.
- NP180783.RALKmlSK6Df6L_e2yFLDOR8kCZATLnnfQNcpyvSh-eneQ130_assertion wasDerivedFrom gad-20150221 NP180783.RALKmlSK6Df6L_e2yFLDOR8kCZATLnnfQNcpyvSh-eneQ130_provenance.
- NP180783.RALKmlSK6Df6L_e2yFLDOR8kCZATLnnfQNcpyvSh-eneQ130_assertion wasGeneratedBy ECO_0000203 NP180783.RALKmlSK6Df6L_e2yFLDOR8kCZATLnnfQNcpyvSh-eneQ130_provenance.
- gad-20150221 importedOn "2015-02-21" NP180783.RALKmlSK6Df6L_e2yFLDOR8kCZATLnnfQNcpyvSh-eneQ130_provenance.