Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP404355.RAyq12q4MVxTfprTWjB6Q8FYW6tuMtceMQb9y_KYb9ngY130_assertion> ?p ?o ?g. }
Showing items 1 to 6 of
6
with 100 items per page.
- NP404355.RAyq12q4MVxTfprTWjB6Q8FYW6tuMtceMQb9y_KYb9ngY130_assertion type Assertion NP404355.RAyq12q4MVxTfprTWjB6Q8FYW6tuMtceMQb9y_KYb9ngY130_head.
- NP404355.RAyq12q4MVxTfprTWjB6Q8FYW6tuMtceMQb9y_KYb9ngY130_assertion description "[Atypical Rett syndrome with selective FOXG1 deletion detected by comparative genomic hybridization: case report and review of literature.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP404355.RAyq12q4MVxTfprTWjB6Q8FYW6tuMtceMQb9y_KYb9ngY130_provenance.
- NP404355.RAyq12q4MVxTfprTWjB6Q8FYW6tuMtceMQb9y_KYb9ngY130_assertion evidence source_evidence_literature NP404355.RAyq12q4MVxTfprTWjB6Q8FYW6tuMtceMQb9y_KYb9ngY130_provenance.
- NP404355.RAyq12q4MVxTfprTWjB6Q8FYW6tuMtceMQb9y_KYb9ngY130_assertion SIO_000772 19623215 NP404355.RAyq12q4MVxTfprTWjB6Q8FYW6tuMtceMQb9y_KYb9ngY130_provenance.
- NP404355.RAyq12q4MVxTfprTWjB6Q8FYW6tuMtceMQb9y_KYb9ngY130_assertion wasDerivedFrom befree-20150227 NP404355.RAyq12q4MVxTfprTWjB6Q8FYW6tuMtceMQb9y_KYb9ngY130_provenance.
- NP404355.RAyq12q4MVxTfprTWjB6Q8FYW6tuMtceMQb9y_KYb9ngY130_assertion wasGeneratedBy ECO_0000203 NP404355.RAyq12q4MVxTfprTWjB6Q8FYW6tuMtceMQb9y_KYb9ngY130_provenance.