Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP79779.RAnVsw7JLf6UjE_90cYqbw7i5im__ymrtgkg4FRxILgN4130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP79779.RAnVsw7JLf6UjE_90cYqbw7i5im__ymrtgkg4FRxILgN4130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP79779.RAnVsw7JLf6UjE_90cYqbw7i5im__ymrtgkg4FRxILgN4130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP79779.RAnVsw7JLf6UjE_90cYqbw7i5im__ymrtgkg4FRxILgN4130_provenance.
- NP79779.RAnVsw7JLf6UjE_90cYqbw7i5im__ymrtgkg4FRxILgN4130_assertion description "[Because single nucleotide polymorphisms (SNPs) are the most subtle genetic variation in the genome, to examine these hypotheses, we have genotyped 30 SNPs in all five NHEJ genes (Ku70, Ku80, DNA-PKcs, Ligase IV, and XRCC4) in 254 primary breast cancer patients and 379 healthy controls.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP79779.RAnVsw7JLf6UjE_90cYqbw7i5im__ymrtgkg4FRxILgN4130_provenance.
- NP79779.RAnVsw7JLf6UjE_90cYqbw7i5im__ymrtgkg4FRxILgN4130_assertion evidence source_evidence_literature NP79779.RAnVsw7JLf6UjE_90cYqbw7i5im__ymrtgkg4FRxILgN4130_provenance.
- NP79779.RAnVsw7JLf6UjE_90cYqbw7i5im__ymrtgkg4FRxILgN4130_assertion SIO_000772 12750264 NP79779.RAnVsw7JLf6UjE_90cYqbw7i5im__ymrtgkg4FRxILgN4130_provenance.
- NP79779.RAnVsw7JLf6UjE_90cYqbw7i5im__ymrtgkg4FRxILgN4130_assertion wasDerivedFrom gad-20150221 NP79779.RAnVsw7JLf6UjE_90cYqbw7i5im__ymrtgkg4FRxILgN4130_provenance.
- NP79779.RAnVsw7JLf6UjE_90cYqbw7i5im__ymrtgkg4FRxILgN4130_assertion wasGeneratedBy ECO_0000203 NP79779.RAnVsw7JLf6UjE_90cYqbw7i5im__ymrtgkg4FRxILgN4130_provenance.
- gad-20150221 importedOn "2015-02-21" NP79779.RAnVsw7JLf6UjE_90cYqbw7i5im__ymrtgkg4FRxILgN4130_provenance.