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- source_evidence_literature type ECO_0000212 NP324325.RACNvn7y2wRA2t7Td_KY83oocLgu6Hqu1e_hzQ5vDp9i0130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP324325.RACNvn7y2wRA2t7Td_KY83oocLgu6Hqu1e_hzQ5vDp9i0130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP324325.RACNvn7y2wRA2t7Td_KY83oocLgu6Hqu1e_hzQ5vDp9i0130_provenance.
- NP324325.RACNvn7y2wRA2t7Td_KY83oocLgu6Hqu1e_hzQ5vDp9i0130_assertion description "[The high Ile(157)--> Thr(157)mutation frequency (6.5%) observed in healthy controls and the lack of other mutations suggest that CHK2 does not contribute significantly to the hereditary breast cancer or LFL-associated breast cancer risk, at least not in the Finnish population.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP324325.RACNvn7y2wRA2t7Td_KY83oocLgu6Hqu1e_hzQ5vDp9i0130_provenance.
- NP324325.RACNvn7y2wRA2t7Td_KY83oocLgu6Hqu1e_hzQ5vDp9i0130_assertion evidence source_evidence_literature NP324325.RACNvn7y2wRA2t7Td_KY83oocLgu6Hqu1e_hzQ5vDp9i0130_provenance.
- NP324325.RACNvn7y2wRA2t7Td_KY83oocLgu6Hqu1e_hzQ5vDp9i0130_assertion SIO_000772 11461078 NP324325.RACNvn7y2wRA2t7Td_KY83oocLgu6Hqu1e_hzQ5vDp9i0130_provenance.
- NP324325.RACNvn7y2wRA2t7Td_KY83oocLgu6Hqu1e_hzQ5vDp9i0130_assertion wasDerivedFrom befree-2016 NP324325.RACNvn7y2wRA2t7Td_KY83oocLgu6Hqu1e_hzQ5vDp9i0130_provenance.
- NP324325.RACNvn7y2wRA2t7Td_KY83oocLgu6Hqu1e_hzQ5vDp9i0130_assertion wasGeneratedBy ECO_0000203 NP324325.RACNvn7y2wRA2t7Td_KY83oocLgu6Hqu1e_hzQ5vDp9i0130_provenance.
- befree-2016 importedOn "2016-02-19" NP324325.RACNvn7y2wRA2t7Td_KY83oocLgu6Hqu1e_hzQ5vDp9i0130_provenance.