Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP592063.RANAifKVJhtkLs7hVh4vVXxQQjSyCpf6qM07ei_wHio3c130_assertion> ?p ?o ?g. }
Showing items 1 to 6 of
6
with 100 items per page.
- NP592063.RANAifKVJhtkLs7hVh4vVXxQQjSyCpf6qM07ei_wHio3c130_assertion type Assertion NP592063.RANAifKVJhtkLs7hVh4vVXxQQjSyCpf6qM07ei_wHio3c130_head.
- NP592063.RANAifKVJhtkLs7hVh4vVXxQQjSyCpf6qM07ei_wHio3c130_assertion description "[Mutations in cohesin complex members SMC3 and SMC1A cause a mild variant of cornelia de Lange syndrome with predominant mental retardation.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP592063.RANAifKVJhtkLs7hVh4vVXxQQjSyCpf6qM07ei_wHio3c130_provenance.
- NP592063.RANAifKVJhtkLs7hVh4vVXxQQjSyCpf6qM07ei_wHio3c130_assertion evidence source_evidence_literature NP592063.RANAifKVJhtkLs7hVh4vVXxQQjSyCpf6qM07ei_wHio3c130_provenance.
- NP592063.RANAifKVJhtkLs7hVh4vVXxQQjSyCpf6qM07ei_wHio3c130_assertion SIO_000772 17273969 NP592063.RANAifKVJhtkLs7hVh4vVXxQQjSyCpf6qM07ei_wHio3c130_provenance.
- NP592063.RANAifKVJhtkLs7hVh4vVXxQQjSyCpf6qM07ei_wHio3c130_assertion wasDerivedFrom befree-2016 NP592063.RANAifKVJhtkLs7hVh4vVXxQQjSyCpf6qM07ei_wHio3c130_provenance.
- NP592063.RANAifKVJhtkLs7hVh4vVXxQQjSyCpf6qM07ei_wHio3c130_assertion wasGeneratedBy ECO_0000203 NP592063.RANAifKVJhtkLs7hVh4vVXxQQjSyCpf6qM07ei_wHio3c130_provenance.