Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP952383.RAFl68H9pe4GJHmBmeG6VjSgFYjFS2117dXIye9tEo9UQ130_assertion> ?p ?o ?g. }
Showing items 1 to 6 of
6
with 100 items per page.
- NP952383.RAFl68H9pe4GJHmBmeG6VjSgFYjFS2117dXIye9tEo9UQ130_assertion type Assertion NP952383.RAFl68H9pe4GJHmBmeG6VjSgFYjFS2117dXIye9tEo9UQ130_head.
- NP952383.RAFl68H9pe4GJHmBmeG6VjSgFYjFS2117dXIye9tEo9UQ130_assertion description "[Based on the previous finding that mutations in COL3A1 cause type IV EDS, our study indicates a possible common pathological pathway linking connective tissue diseases and brain malformations.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP952383.RAFl68H9pe4GJHmBmeG6VjSgFYjFS2117dXIye9tEo9UQ130_provenance.
- NP952383.RAFl68H9pe4GJHmBmeG6VjSgFYjFS2117dXIye9tEo9UQ130_assertion evidence source_evidence_literature NP952383.RAFl68H9pe4GJHmBmeG6VjSgFYjFS2117dXIye9tEo9UQ130_provenance.
- NP952383.RAFl68H9pe4GJHmBmeG6VjSgFYjFS2117dXIye9tEo9UQ130_assertion SIO_000772 22235340 NP952383.RAFl68H9pe4GJHmBmeG6VjSgFYjFS2117dXIye9tEo9UQ130_provenance.
- NP952383.RAFl68H9pe4GJHmBmeG6VjSgFYjFS2117dXIye9tEo9UQ130_assertion wasDerivedFrom befree-2016 NP952383.RAFl68H9pe4GJHmBmeG6VjSgFYjFS2117dXIye9tEo9UQ130_provenance.
- NP952383.RAFl68H9pe4GJHmBmeG6VjSgFYjFS2117dXIye9tEo9UQ130_assertion wasGeneratedBy ECO_0000203 NP952383.RAFl68H9pe4GJHmBmeG6VjSgFYjFS2117dXIye9tEo9UQ130_provenance.