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- NP625881.RAqazs6whC5Vv-Urqjs_30GfMfhl_P8AbCN6K8la9hl4Q130_assertion type Assertion NP625881.RAqazs6whC5Vv-Urqjs_30GfMfhl_P8AbCN6K8la9hl4Q130_head.
- NP625881.RAqazs6whC5Vv-Urqjs_30GfMfhl_P8AbCN6K8la9hl4Q130_assertion description "[Wolcott-Rallison syndrome (WRS) is caused by recessive EIF2AK3 gene mutations and characterized by permanent neonatal diabetes (PNDM), skeletal dysplasia, and recurrent hepatitis.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP625881.RAqazs6whC5Vv-Urqjs_30GfMfhl_P8AbCN6K8la9hl4Q130_provenance.
- NP625881.RAqazs6whC5Vv-Urqjs_30GfMfhl_P8AbCN6K8la9hl4Q130_assertion evidence source_evidence_literature NP625881.RAqazs6whC5Vv-Urqjs_30GfMfhl_P8AbCN6K8la9hl4Q130_provenance.
- NP625881.RAqazs6whC5Vv-Urqjs_30GfMfhl_P8AbCN6K8la9hl4Q130_assertion SIO_000772 23759358 NP625881.RAqazs6whC5Vv-Urqjs_30GfMfhl_P8AbCN6K8la9hl4Q130_provenance.
- NP625881.RAqazs6whC5Vv-Urqjs_30GfMfhl_P8AbCN6K8la9hl4Q130_assertion wasDerivedFrom befree-20140225 NP625881.RAqazs6whC5Vv-Urqjs_30GfMfhl_P8AbCN6K8la9hl4Q130_provenance.
- NP625881.RAqazs6whC5Vv-Urqjs_30GfMfhl_P8AbCN6K8la9hl4Q130_assertion wasGeneratedBy ECO_0000203 NP625881.RAqazs6whC5Vv-Urqjs_30GfMfhl_P8AbCN6K8la9hl4Q130_provenance.