Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP1087928.RAmpHDdNvJCbgsN3jWBHIKv8kaRQSy7cgyWeb_L5NCalk130_assertion> ?p ?o ?g. }
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- NP1087928.RAmpHDdNvJCbgsN3jWBHIKv8kaRQSy7cgyWeb_L5NCalk130_assertion type Assertion NP1087928.RAmpHDdNvJCbgsN3jWBHIKv8kaRQSy7cgyWeb_L5NCalk130_head.
- NP1087928.RAmpHDdNvJCbgsN3jWBHIKv8kaRQSy7cgyWeb_L5NCalk130_assertion description "[Furthermore, our sibling pair highlights the intrafamilial variability, the natural clinical course of ALG3-CDG (CDG-Id) and the benefit of reassessing patients with undiagnosed and complex syndromes, particularly when they present with neurological deterioration.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1087928.RAmpHDdNvJCbgsN3jWBHIKv8kaRQSy7cgyWeb_L5NCalk130_provenance.
- NP1087928.RAmpHDdNvJCbgsN3jWBHIKv8kaRQSy7cgyWeb_L5NCalk130_assertion evidence source_evidence_literature NP1087928.RAmpHDdNvJCbgsN3jWBHIKv8kaRQSy7cgyWeb_L5NCalk130_provenance.
- NP1087928.RAmpHDdNvJCbgsN3jWBHIKv8kaRQSy7cgyWeb_L5NCalk130_assertion SIO_000772 23791010 NP1087928.RAmpHDdNvJCbgsN3jWBHIKv8kaRQSy7cgyWeb_L5NCalk130_provenance.
- NP1087928.RAmpHDdNvJCbgsN3jWBHIKv8kaRQSy7cgyWeb_L5NCalk130_assertion wasDerivedFrom befree-2016 NP1087928.RAmpHDdNvJCbgsN3jWBHIKv8kaRQSy7cgyWeb_L5NCalk130_provenance.
- NP1087928.RAmpHDdNvJCbgsN3jWBHIKv8kaRQSy7cgyWeb_L5NCalk130_assertion wasGeneratedBy ECO_0000203 NP1087928.RAmpHDdNvJCbgsN3jWBHIKv8kaRQSy7cgyWeb_L5NCalk130_provenance.