Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP20971.RA4lxm32Hy5kCN-IkH6RrZ8LvzvcF-49ayxdeubrlJ7l8130_assertion> ?p ?o ?g. }
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- NP20971.RA4lxm32Hy5kCN-IkH6RrZ8LvzvcF-49ayxdeubrlJ7l8130_assertion type Assertion NP20971.RA4lxm32Hy5kCN-IkH6RrZ8LvzvcF-49ayxdeubrlJ7l8130_head.
- NP20971.RA4lxm32Hy5kCN-IkH6RrZ8LvzvcF-49ayxdeubrlJ7l8130_assertion wasGeneratedBy ECO_0000218 NP20971.RA4lxm32Hy5kCN-IkH6RrZ8LvzvcF-49ayxdeubrlJ7l8130_provenance.
- NP20971.RA4lxm32Hy5kCN-IkH6RrZ8LvzvcF-49ayxdeubrlJ7l8130_assertion wasDerivedFrom ctd_human-2016 NP20971.RA4lxm32Hy5kCN-IkH6RrZ8LvzvcF-49ayxdeubrlJ7l8130_provenance.
- NP20971.RA4lxm32Hy5kCN-IkH6RrZ8LvzvcF-49ayxdeubrlJ7l8130_assertion SIO_000772 18162506 NP20971.RA4lxm32Hy5kCN-IkH6RrZ8LvzvcF-49ayxdeubrlJ7l8130_provenance.
- NP20971.RA4lxm32Hy5kCN-IkH6RrZ8LvzvcF-49ayxdeubrlJ7l8130_assertion evidence source_evidence_curated NP20971.RA4lxm32Hy5kCN-IkH6RrZ8LvzvcF-49ayxdeubrlJ7l8130_provenance.
- NP20971.RA4lxm32Hy5kCN-IkH6RrZ8LvzvcF-49ayxdeubrlJ7l8130_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." NP20971.RA4lxm32Hy5kCN-IkH6RrZ8LvzvcF-49ayxdeubrlJ7l8130_provenance.