Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP908690.RAcbtEZ0_9t6KWrs_rxV1ulu9MJXRKrfQ4hKV3ArCwQ8Q130_assertion> ?p ?o ?g. }
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- NP908690.RAcbtEZ0_9t6KWrs_rxV1ulu9MJXRKrfQ4hKV3ArCwQ8Q130_assertion type Assertion NP908690.RAcbtEZ0_9t6KWrs_rxV1ulu9MJXRKrfQ4hKV3ArCwQ8Q130_head.
- NP908690.RAcbtEZ0_9t6KWrs_rxV1ulu9MJXRKrfQ4hKV3ArCwQ8Q130_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." NP908690.RAcbtEZ0_9t6KWrs_rxV1ulu9MJXRKrfQ4hKV3ArCwQ8Q130_provenance.
- NP908690.RAcbtEZ0_9t6KWrs_rxV1ulu9MJXRKrfQ4hKV3ArCwQ8Q130_assertion evidence source_evidence_literature NP908690.RAcbtEZ0_9t6KWrs_rxV1ulu9MJXRKrfQ4hKV3ArCwQ8Q130_provenance.
- NP908690.RAcbtEZ0_9t6KWrs_rxV1ulu9MJXRKrfQ4hKV3ArCwQ8Q130_assertion SIO_000772 15851739 NP908690.RAcbtEZ0_9t6KWrs_rxV1ulu9MJXRKrfQ4hKV3ArCwQ8Q130_provenance.
- NP908690.RAcbtEZ0_9t6KWrs_rxV1ulu9MJXRKrfQ4hKV3ArCwQ8Q130_assertion wasDerivedFrom befree-20140225 NP908690.RAcbtEZ0_9t6KWrs_rxV1ulu9MJXRKrfQ4hKV3ArCwQ8Q130_provenance.
- NP908690.RAcbtEZ0_9t6KWrs_rxV1ulu9MJXRKrfQ4hKV3ArCwQ8Q130_assertion wasGeneratedBy ECO_0000203 NP908690.RAcbtEZ0_9t6KWrs_rxV1ulu9MJXRKrfQ4hKV3ArCwQ8Q130_provenance.