Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP116913.RA18S_DfXoZLG3pzvQKiJjEN1uFTxFqzXeOeSj8nloCgM130_assertion> ?p ?o ?g. }
Showing items 1 to 6 of
6
with 100 items per page.
- NP116913.RA18S_DfXoZLG3pzvQKiJjEN1uFTxFqzXeOeSj8nloCgM130_assertion type Assertion NP116913.RA18S_DfXoZLG3pzvQKiJjEN1uFTxFqzXeOeSj8nloCgM130_head.
- 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.