Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP779377.RAgHDR6bpfFoV0q-XE3uE_rxyVfo2k-TgIdS-TMffmyWM130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP779377.RAgHDR6bpfFoV0q-XE3uE_rxyVfo2k-TgIdS-TMffmyWM130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP779377.RAgHDR6bpfFoV0q-XE3uE_rxyVfo2k-TgIdS-TMffmyWM130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP779377.RAgHDR6bpfFoV0q-XE3uE_rxyVfo2k-TgIdS-TMffmyWM130_provenance.
- NP779377.RAgHDR6bpfFoV0q-XE3uE_rxyVfo2k-TgIdS-TMffmyWM130_assertion description "[This is the first report on the studies of XPC and XRCC1 Arg194Trp polymorphisms in PC, and our present data suggest that XPC Lys939Gln and the T-A haplotype of XRCC1 Arg194Trp and Arg399Gln may be risk factors for PC in Japanese.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP779377.RAgHDR6bpfFoV0q-XE3uE_rxyVfo2k-TgIdS-TMffmyWM130_provenance.
- NP779377.RAgHDR6bpfFoV0q-XE3uE_rxyVfo2k-TgIdS-TMffmyWM130_assertion evidence source_evidence_literature NP779377.RAgHDR6bpfFoV0q-XE3uE_rxyVfo2k-TgIdS-TMffmyWM130_provenance.
- NP779377.RAgHDR6bpfFoV0q-XE3uE_rxyVfo2k-TgIdS-TMffmyWM130_assertion SIO_000772 17196815 NP779377.RAgHDR6bpfFoV0q-XE3uE_rxyVfo2k-TgIdS-TMffmyWM130_provenance.
- NP779377.RAgHDR6bpfFoV0q-XE3uE_rxyVfo2k-TgIdS-TMffmyWM130_assertion wasDerivedFrom befree-20150227 NP779377.RAgHDR6bpfFoV0q-XE3uE_rxyVfo2k-TgIdS-TMffmyWM130_provenance.
- NP779377.RAgHDR6bpfFoV0q-XE3uE_rxyVfo2k-TgIdS-TMffmyWM130_assertion wasGeneratedBy ECO_0000203 NP779377.RAgHDR6bpfFoV0q-XE3uE_rxyVfo2k-TgIdS-TMffmyWM130_provenance.
- befree-20150227 importedOn "2015-02-27" NP779377.RAgHDR6bpfFoV0q-XE3uE_rxyVfo2k-TgIdS-TMffmyWM130_provenance.