Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP3270.RAK2wUnKitolCzKC9KmpgkqeOrrBu6dOc4vd6ceDYqSM0130_assertion> ?p ?o ?g. }
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- NP3270.RAK2wUnKitolCzKC9KmpgkqeOrrBu6dOc4vd6ceDYqSM0130_assertion type Assertion NP3270.RAK2wUnKitolCzKC9KmpgkqeOrrBu6dOc4vd6ceDYqSM0130_head.
- NP3270.RAK2wUnKitolCzKC9KmpgkqeOrrBu6dOc4vd6ceDYqSM0130_assertion wasGeneratedBy ECO_0000218 NP3270.RAK2wUnKitolCzKC9KmpgkqeOrrBu6dOc4vd6ceDYqSM0130_provenance.
- NP3270.RAK2wUnKitolCzKC9KmpgkqeOrrBu6dOc4vd6ceDYqSM0130_assertion wasDerivedFrom uniprot-20130724 NP3270.RAK2wUnKitolCzKC9KmpgkqeOrrBu6dOc4vd6ceDYqSM0130_provenance.
- NP3270.RAK2wUnKitolCzKC9KmpgkqeOrrBu6dOc4vd6ceDYqSM0130_assertion SIO_000772 18162506 NP3270.RAK2wUnKitolCzKC9KmpgkqeOrrBu6dOc4vd6ceDYqSM0130_provenance.
- NP3270.RAK2wUnKitolCzKC9KmpgkqeOrrBu6dOc4vd6ceDYqSM0130_assertion evidence source_evidence_curated NP3270.RAK2wUnKitolCzKC9KmpgkqeOrrBu6dOc4vd6ceDYqSM0130_provenance.
- NP3270.RAK2wUnKitolCzKC9KmpgkqeOrrBu6dOc4vd6ceDYqSM0130_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." NP3270.RAK2wUnKitolCzKC9KmpgkqeOrrBu6dOc4vd6ceDYqSM0130_provenance.