Matches in Nanopublications for { ?s ?p "[Cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy (CADASIL) is a heritable small-vessel disease caused by mutations in NOTCH3 gene and clinically characterized 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. }
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- NP564838.RAh8bvT1P2r4Sa6EXZe0b-mFmvNzExXR41QBw2bNQnmBY130_assertion description "[Cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy (CADASIL) is a heritable small-vessel disease caused by mutations in NOTCH3 gene and clinically characterized 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." NP564838.RAh8bvT1P2r4Sa6EXZe0b-mFmvNzExXR41QBw2bNQnmBY130_provenance.
- NP835496.RAXN9_ZnoSyPwM3RQ560a4r96PXjYU3egaPqCMKAgUrGo130_assertion description "[Cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy (CADASIL) is a heritable small-vessel disease caused by mutations in NOTCH3 gene and clinically characterized 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." NP835496.RAXN9_ZnoSyPwM3RQ560a4r96PXjYU3egaPqCMKAgUrGo130_provenance.
- NP436368.RA_uTLnxiOsjaG3loETVXewavRl6JJJk6W0IZMvJVcJwU130_assertion description "[Cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy (CADASIL) is a heritable small-vessel disease caused by mutations in NOTCH3 gene and clinically characterized 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." NP436368.RA_uTLnxiOsjaG3loETVXewavRl6JJJk6W0IZMvJVcJwU130_provenance.
- NP651448.RA8tAlYykDQRyNw530b139xA6qvQEeJ2kpYfZ0Gd0-NfY130_assertion description "[Cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy (CADASIL) is a heritable small-vessel disease caused by mutations in NOTCH3 gene and clinically characterized 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." NP651448.RA8tAlYykDQRyNw530b139xA6qvQEeJ2kpYfZ0Gd0-NfY130_provenance.
- NP909034.RAOIDfOn0h6vlUP6n6vSGT1ERcqp1WTo26rvAt7BbNiCg130_assertion description "[Cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy (CADASIL) is a heritable small-vessel disease caused by mutations in NOTCH3 gene and clinically characterized 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." NP909034.RAOIDfOn0h6vlUP6n6vSGT1ERcqp1WTo26rvAt7BbNiCg130_provenance.