Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP1087928.RAmpHDdNvJCbgsN3jWBHIKv8kaRQSy7cgyWeb_L5NCalk130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP1087928.RAmpHDdNvJCbgsN3jWBHIKv8kaRQSy7cgyWeb_L5NCalk130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP1087928.RAmpHDdNvJCbgsN3jWBHIKv8kaRQSy7cgyWeb_L5NCalk130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP1087928.RAmpHDdNvJCbgsN3jWBHIKv8kaRQSy7cgyWeb_L5NCalk130_provenance.
- 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.
- befree-2016 importedOn "2016-02-19" NP1087928.RAmpHDdNvJCbgsN3jWBHIKv8kaRQSy7cgyWeb_L5NCalk130_provenance.