Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP718211.RAps6oCy3c4D8a7lxJBijXdGV25BCsEP9Z6rv6mA1qZHc130_assertion> ?p ?o ?g. }
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- NP718211.RAps6oCy3c4D8a7lxJBijXdGV25BCsEP9Z6rv6mA1qZHc130_assertion type Assertion NP718211.RAps6oCy3c4D8a7lxJBijXdGV25BCsEP9Z6rv6mA1qZHc130_head.
- NP718211.RAps6oCy3c4D8a7lxJBijXdGV25BCsEP9Z6rv6mA1qZHc130_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." NP718211.RAps6oCy3c4D8a7lxJBijXdGV25BCsEP9Z6rv6mA1qZHc130_provenance.
- NP718211.RAps6oCy3c4D8a7lxJBijXdGV25BCsEP9Z6rv6mA1qZHc130_assertion evidence source_evidence_literature NP718211.RAps6oCy3c4D8a7lxJBijXdGV25BCsEP9Z6rv6mA1qZHc130_provenance.
- NP718211.RAps6oCy3c4D8a7lxJBijXdGV25BCsEP9Z6rv6mA1qZHc130_assertion SIO_000772 15851739 NP718211.RAps6oCy3c4D8a7lxJBijXdGV25BCsEP9Z6rv6mA1qZHc130_provenance.
- NP718211.RAps6oCy3c4D8a7lxJBijXdGV25BCsEP9Z6rv6mA1qZHc130_assertion wasDerivedFrom befree-20140225 NP718211.RAps6oCy3c4D8a7lxJBijXdGV25BCsEP9Z6rv6mA1qZHc130_provenance.
- NP718211.RAps6oCy3c4D8a7lxJBijXdGV25BCsEP9Z6rv6mA1qZHc130_assertion wasGeneratedBy ECO_0000203 NP718211.RAps6oCy3c4D8a7lxJBijXdGV25BCsEP9Z6rv6mA1qZHc130_provenance.