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- NP909034.RAOIDfOn0h6vlUP6n6vSGT1ERcqp1WTo26rvAt7BbNiCg130_assertion type Assertion NP909034.RAOIDfOn0h6vlUP6n6vSGT1ERcqp1WTo26rvAt7BbNiCg130_head.
- 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.
- NP909034.RAOIDfOn0h6vlUP6n6vSGT1ERcqp1WTo26rvAt7BbNiCg130_assertion evidence source_evidence_literature NP909034.RAOIDfOn0h6vlUP6n6vSGT1ERcqp1WTo26rvAt7BbNiCg130_provenance.
- NP909034.RAOIDfOn0h6vlUP6n6vSGT1ERcqp1WTo26rvAt7BbNiCg130_assertion SIO_000772 19576955 NP909034.RAOIDfOn0h6vlUP6n6vSGT1ERcqp1WTo26rvAt7BbNiCg130_provenance.
- NP909034.RAOIDfOn0h6vlUP6n6vSGT1ERcqp1WTo26rvAt7BbNiCg130_assertion wasDerivedFrom befree-20140225 NP909034.RAOIDfOn0h6vlUP6n6vSGT1ERcqp1WTo26rvAt7BbNiCg130_provenance.
- NP909034.RAOIDfOn0h6vlUP6n6vSGT1ERcqp1WTo26rvAt7BbNiCg130_assertion wasGeneratedBy ECO_0000203 NP909034.RAOIDfOn0h6vlUP6n6vSGT1ERcqp1WTo26rvAt7BbNiCg130_provenance.