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- NP596324.RAYehc4N2lcOAwIgjCsO5Q1QSE56haRbAMfXwzTxERsAg130_assertion type Assertion NP596324.RAYehc4N2lcOAwIgjCsO5Q1QSE56haRbAMfXwzTxERsAg130_head.
- NP596324.RAYehc4N2lcOAwIgjCsO5Q1QSE56haRbAMfXwzTxERsAg130_assertion description "[Based on a structured questionnaire and medical records, the authors found that 12 of 25 mothers with cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy (CADASIL) with the R133C NOTCH3 mutation had had neurologic symptoms in 17 of their 43 pregnancies, most commonly hemiparesthesia (76%), hemiparesis (36%), aphasia (65%), and visual disorders (47%).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP596324.RAYehc4N2lcOAwIgjCsO5Q1QSE56haRbAMfXwzTxERsAg130_provenance.
- NP596324.RAYehc4N2lcOAwIgjCsO5Q1QSE56haRbAMfXwzTxERsAg130_assertion evidence source_evidence_literature NP596324.RAYehc4N2lcOAwIgjCsO5Q1QSE56haRbAMfXwzTxERsAg130_provenance.
- NP596324.RAYehc4N2lcOAwIgjCsO5Q1QSE56haRbAMfXwzTxERsAg130_assertion SIO_000772 15851739 NP596324.RAYehc4N2lcOAwIgjCsO5Q1QSE56haRbAMfXwzTxERsAg130_provenance.
- NP596324.RAYehc4N2lcOAwIgjCsO5Q1QSE56haRbAMfXwzTxERsAg130_assertion wasDerivedFrom befree-20150227 NP596324.RAYehc4N2lcOAwIgjCsO5Q1QSE56haRbAMfXwzTxERsAg130_provenance.
- NP596324.RAYehc4N2lcOAwIgjCsO5Q1QSE56haRbAMfXwzTxERsAg130_assertion wasGeneratedBy ECO_0000203 NP596324.RAYehc4N2lcOAwIgjCsO5Q1QSE56haRbAMfXwzTxERsAg130_provenance.