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- source_evidence_literature type ECO_0000212 NP116913.RA18S_DfXoZLG3pzvQKiJjEN1uFTxFqzXeOeSj8nloCgM130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP116913.RA18S_DfXoZLG3pzvQKiJjEN1uFTxFqzXeOeSj8nloCgM130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP116913.RA18S_DfXoZLG3pzvQKiJjEN1uFTxFqzXeOeSj8nloCgM130_provenance.
- gad-20150221 importedOn "2015-02-21" NP116913.RA18S_DfXoZLG3pzvQKiJjEN1uFTxFqzXeOeSj8nloCgM130_provenance.
- NP116913.RA18S_DfXoZLG3pzvQKiJjEN1uFTxFqzXeOeSj8nloCgM130_assertion wasGeneratedBy ECO_0000203 NP116913.RA18S_DfXoZLG3pzvQKiJjEN1uFTxFqzXeOeSj8nloCgM130_provenance.
- NP116913.RA18S_DfXoZLG3pzvQKiJjEN1uFTxFqzXeOeSj8nloCgM130_assertion wasDerivedFrom gad-20150221 NP116913.RA18S_DfXoZLG3pzvQKiJjEN1uFTxFqzXeOeSj8nloCgM130_provenance.
- NP116913.RA18S_DfXoZLG3pzvQKiJjEN1uFTxFqzXeOeSj8nloCgM130_assertion SIO_000772 18162506 NP116913.RA18S_DfXoZLG3pzvQKiJjEN1uFTxFqzXeOeSj8nloCgM130_provenance.
- NP116913.RA18S_DfXoZLG3pzvQKiJjEN1uFTxFqzXeOeSj8nloCgM130_assertion evidence source_evidence_literature NP116913.RA18S_DfXoZLG3pzvQKiJjEN1uFTxFqzXeOeSj8nloCgM130_provenance.
- NP116913.RA18S_DfXoZLG3pzvQKiJjEN1uFTxFqzXeOeSj8nloCgM130_assertion description "[Insulin mutation screening in 1,044 patients with diabetes: mutations in the INS gene are a common cause of neonatal diabetes but a rare cause of diabetes diagnosed in childhood or adulthood.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP116913.RA18S_DfXoZLG3pzvQKiJjEN1uFTxFqzXeOeSj8nloCgM130_provenance.