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Matches in Nanopublications for { ?s ?p "[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."@en ?g. }

• NP556039.RAAo14NuoLTKNz2rxcGq_iY0iBKvKcO-UtWv74UVHAjvg130_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." NP556039.RAAo14NuoLTKNz2rxcGq_iY0iBKvKcO-UtWv74UVHAjvg130_provenance.
• 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.
• NP548197.RAZ74dKyE3NzbNvobOjzq4_9N-upkhc7vpcH8-j7HivzM130_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." NP548197.RAZ74dKyE3NzbNvobOjzq4_9N-upkhc7vpcH8-j7HivzM130_provenance.
• NP783671.RAW8AzJb0AZSVJHzhLy9JRE2NwKjqx-ZbDN9M0MPYVi58130_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." NP783671.RAW8AzJb0AZSVJHzhLy9JRE2NwKjqx-ZbDN9M0MPYVi58130_provenance.
• NP422488.RAWmiVr93qGCy2HMvUcgMjKInijvarMerwTA6m04Aue34130_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." NP422488.RAWmiVr93qGCy2HMvUcgMjKInijvarMerwTA6m04Aue34130_provenance.
• NP401107.RA1u9EWwrfbh51KJwGOT8Zck5gd_WSU5SrQyga_MrzBHQ130_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." NP401107.RA1u9EWwrfbh51KJwGOT8Zck5gd_WSU5SrQyga_MrzBHQ130_provenance.
• NP294155.RAz5H1xazDQPkJtAbv0Flbt6PNpJzTrYHejySf9UkvRaE130_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." NP294155.RAz5H1xazDQPkJtAbv0Flbt6PNpJzTrYHejySf9UkvRaE130_provenance.
• NP675448.RA2sXcLNAf6qFN7tEOEoI2BP-ovfkeChs0DFC2u5oEZOA130_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." NP675448.RA2sXcLNAf6qFN7tEOEoI2BP-ovfkeChs0DFC2u5oEZOA130_provenance.
• NP807390.RA2gPYMPgOIH3FEGeYP6lUp60XwudKiNpQ2tCFtWEH3_s130_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." NP807390.RA2gPYMPgOIH3FEGeYP6lUp60XwudKiNpQ2tCFtWEH3_s130_provenance.
• NP596363.RAQBgobIBdAmwBqej5jn1xhUKu9guUE-eJQnMFcGaBhjA130_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." NP596363.RAQBgobIBdAmwBqej5jn1xhUKu9guUE-eJQnMFcGaBhjA130_provenance.
• NP596598.RAaWAPUZCEvjd9oO3gTStgvh6hBRb3NBb0cEK8CeJY-2s130_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." NP596598.RAaWAPUZCEvjd9oO3gTStgvh6hBRb3NBb0cEK8CeJY-2s130_provenance.
• NP895412.RA-8IcwynP7vT_vBIs-6hXnWSmnjrbPICJzU1EZ1wngVI130_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." NP895412.RA-8IcwynP7vT_vBIs-6hXnWSmnjrbPICJzU1EZ1wngVI130_provenance.
• 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." provenance.
• 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." provenance.
• 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." provenance.
• 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." provenance.
• NP906005.RAEvjNNcWY-QQUHG08YtoHVz2LLI60s0Aj6yQ-VNOSUZo130_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." NP906005.RAEvjNNcWY-QQUHG08YtoHVz2LLI60s0Aj6yQ-VNOSUZo130_provenance.
• NP557224.RAan7MxulkbzeuEvWHYm85rKTJRd0s31NJoDe2GQNs4Vw130_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." NP557224.RAan7MxulkbzeuEvWHYm85rKTJRd0s31NJoDe2GQNs4Vw130_provenance.
• NP557225.RASFiyeJpR0polxAple67NNzvpBj7pUZyifunIG8eHJ48130_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." NP557225.RASFiyeJpR0polxAple67NNzvpBj7pUZyifunIG8eHJ48130_provenance.
• NP596541.RAKZ92efnwYvXoRsPdV7dnEW8fEAiBnSOx-WyKOCDTDtE130_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." NP596541.RAKZ92efnwYvXoRsPdV7dnEW8fEAiBnSOx-WyKOCDTDtE130_provenance.
• NP557223.RAHloPDHP8La9nkMKnLSiT5S-AvN34i39hofOpVJ7fPa8130_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." NP557223.RAHloPDHP8La9nkMKnLSiT5S-AvN34i39hofOpVJ7fPa8130_provenance.