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- NP844356.RABWlUulZ_XRLrSe-y1U9zQFjVAycBlil3HsG_xEbX1-M130_assertion type Assertion NP844356.RABWlUulZ_XRLrSe-y1U9zQFjVAycBlil3HsG_xEbX1-M130_head.
- NP844356.RABWlUulZ_XRLrSe-y1U9zQFjVAycBlil3HsG_xEbX1-M130_assertion description "[Mutations in the NOTCH3 gene cause cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy (CADASIL), which is clinically characterised by recurrent ischemic strokes, migraine with aura, psychiatric symptoms, cognitive decline and dementia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP844356.RABWlUulZ_XRLrSe-y1U9zQFjVAycBlil3HsG_xEbX1-M130_provenance.
- NP844356.RABWlUulZ_XRLrSe-y1U9zQFjVAycBlil3HsG_xEbX1-M130_assertion evidence source_evidence_literature NP844356.RABWlUulZ_XRLrSe-y1U9zQFjVAycBlil3HsG_xEbX1-M130_provenance.
- NP844356.RABWlUulZ_XRLrSe-y1U9zQFjVAycBlil3HsG_xEbX1-M130_assertion SIO_000772 16807713 NP844356.RABWlUulZ_XRLrSe-y1U9zQFjVAycBlil3HsG_xEbX1-M130_provenance.
- NP844356.RABWlUulZ_XRLrSe-y1U9zQFjVAycBlil3HsG_xEbX1-M130_assertion wasDerivedFrom befree-20140225 NP844356.RABWlUulZ_XRLrSe-y1U9zQFjVAycBlil3HsG_xEbX1-M130_provenance.
- NP844356.RABWlUulZ_XRLrSe-y1U9zQFjVAycBlil3HsG_xEbX1-M130_assertion wasGeneratedBy ECO_0000203 NP844356.RABWlUulZ_XRLrSe-y1U9zQFjVAycBlil3HsG_xEbX1-M130_provenance.