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- NP647321.RAhLKHaTRXYBNHUWc8NsOJND7F7C1GdegiczlBRwc-dig130_assertion type Assertion NP647321.RAhLKHaTRXYBNHUWc8NsOJND7F7C1GdegiczlBRwc-dig130_head.
- NP647321.RAhLKHaTRXYBNHUWc8NsOJND7F7C1GdegiczlBRwc-dig130_assertion wasGeneratedBy ECO_0000203 NP647321.RAhLKHaTRXYBNHUWc8NsOJND7F7C1GdegiczlBRwc-dig130_provenance.
- NP647321.RAhLKHaTRXYBNHUWc8NsOJND7F7C1GdegiczlBRwc-dig130_assertion wasDerivedFrom befree-2016 NP647321.RAhLKHaTRXYBNHUWc8NsOJND7F7C1GdegiczlBRwc-dig130_provenance.
- NP647321.RAhLKHaTRXYBNHUWc8NsOJND7F7C1GdegiczlBRwc-dig130_assertion SIO_000772 18162506 NP647321.RAhLKHaTRXYBNHUWc8NsOJND7F7C1GdegiczlBRwc-dig130_provenance.
- NP647321.RAhLKHaTRXYBNHUWc8NsOJND7F7C1GdegiczlBRwc-dig130_assertion evidence source_evidence_literature NP647321.RAhLKHaTRXYBNHUWc8NsOJND7F7C1GdegiczlBRwc-dig130_provenance.
- NP647321.RAhLKHaTRXYBNHUWc8NsOJND7F7C1GdegiczlBRwc-dig130_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." NP647321.RAhLKHaTRXYBNHUWc8NsOJND7F7C1GdegiczlBRwc-dig130_provenance.