Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP596502.RAV_f7SBOcEryXAZMmbB4-rschir0hY8S7ekmdlKJgyWw130_assertion> ?p ?o ?g. }
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- NP596502.RAV_f7SBOcEryXAZMmbB4-rschir0hY8S7ekmdlKJgyWw130_assertion type Assertion NP596502.RAV_f7SBOcEryXAZMmbB4-rschir0hY8S7ekmdlKJgyWw130_head.
- NP596502.RAV_f7SBOcEryXAZMmbB4-rschir0hY8S7ekmdlKJgyWw130_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." NP596502.RAV_f7SBOcEryXAZMmbB4-rschir0hY8S7ekmdlKJgyWw130_provenance.
- NP596502.RAV_f7SBOcEryXAZMmbB4-rschir0hY8S7ekmdlKJgyWw130_assertion evidence source_evidence_literature NP596502.RAV_f7SBOcEryXAZMmbB4-rschir0hY8S7ekmdlKJgyWw130_provenance.
- NP596502.RAV_f7SBOcEryXAZMmbB4-rschir0hY8S7ekmdlKJgyWw130_assertion SIO_000772 15851739 NP596502.RAV_f7SBOcEryXAZMmbB4-rschir0hY8S7ekmdlKJgyWw130_provenance.
- NP596502.RAV_f7SBOcEryXAZMmbB4-rschir0hY8S7ekmdlKJgyWw130_assertion wasDerivedFrom befree-20150227 NP596502.RAV_f7SBOcEryXAZMmbB4-rschir0hY8S7ekmdlKJgyWw130_provenance.
- NP596502.RAV_f7SBOcEryXAZMmbB4-rschir0hY8S7ekmdlKJgyWw130_assertion wasGeneratedBy ECO_0000203 NP596502.RAV_f7SBOcEryXAZMmbB4-rschir0hY8S7ekmdlKJgyWw130_provenance.