Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP491457.RAar7AFbFOiVe97Mgg0Xq3u3dvP2OL8eF_rs8wpLH5ngk130_assertion> ?p ?o ?g. }
Showing items 1 to 6 of
6
with 100 items per page.
- NP491457.RAar7AFbFOiVe97Mgg0Xq3u3dvP2OL8eF_rs8wpLH5ngk130_assertion type Assertion NP491457.RAar7AFbFOiVe97Mgg0Xq3u3dvP2OL8eF_rs8wpLH5ngk130_head.
- NP491457.RAar7AFbFOiVe97Mgg0Xq3u3dvP2OL8eF_rs8wpLH5ngk130_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." NP491457.RAar7AFbFOiVe97Mgg0Xq3u3dvP2OL8eF_rs8wpLH5ngk130_provenance.
- NP491457.RAar7AFbFOiVe97Mgg0Xq3u3dvP2OL8eF_rs8wpLH5ngk130_assertion evidence source_evidence_literature NP491457.RAar7AFbFOiVe97Mgg0Xq3u3dvP2OL8eF_rs8wpLH5ngk130_provenance.
- NP491457.RAar7AFbFOiVe97Mgg0Xq3u3dvP2OL8eF_rs8wpLH5ngk130_assertion SIO_000772 15851739 NP491457.RAar7AFbFOiVe97Mgg0Xq3u3dvP2OL8eF_rs8wpLH5ngk130_provenance.
- NP491457.RAar7AFbFOiVe97Mgg0Xq3u3dvP2OL8eF_rs8wpLH5ngk130_assertion wasDerivedFrom befree-2016 NP491457.RAar7AFbFOiVe97Mgg0Xq3u3dvP2OL8eF_rs8wpLH5ngk130_provenance.
- NP491457.RAar7AFbFOiVe97Mgg0Xq3u3dvP2OL8eF_rs8wpLH5ngk130_assertion wasGeneratedBy ECO_0000203 NP491457.RAar7AFbFOiVe97Mgg0Xq3u3dvP2OL8eF_rs8wpLH5ngk130_provenance.