Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP723405.RA8AYGpI0kyrO-7lX5jIqYNwj4iBao7cWmAcKPlj2aj2c130_assertion> ?p ?o ?g. }
Showing items 1 to 6 of
6
with 100 items per page.
- NP723405.RA8AYGpI0kyrO-7lX5jIqYNwj4iBao7cWmAcKPlj2aj2c130_assertion type Assertion NP723405.RA8AYGpI0kyrO-7lX5jIqYNwj4iBao7cWmAcKPlj2aj2c130_head.
- NP723405.RA8AYGpI0kyrO-7lX5jIqYNwj4iBao7cWmAcKPlj2aj2c130_assertion description "[The TBX1 gene is considered to be the major candidate gene for the main features in 22q11.2 deletion syndrome, including congenital heart malformations, (para)thyroid hypoplasia, and craniofacial abnormalities.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP723405.RA8AYGpI0kyrO-7lX5jIqYNwj4iBao7cWmAcKPlj2aj2c130_provenance.
- NP723405.RA8AYGpI0kyrO-7lX5jIqYNwj4iBao7cWmAcKPlj2aj2c130_assertion evidence source_evidence_literature NP723405.RA8AYGpI0kyrO-7lX5jIqYNwj4iBao7cWmAcKPlj2aj2c130_provenance.
- NP723405.RA8AYGpI0kyrO-7lX5jIqYNwj4iBao7cWmAcKPlj2aj2c130_assertion SIO_000772 22893440 NP723405.RA8AYGpI0kyrO-7lX5jIqYNwj4iBao7cWmAcKPlj2aj2c130_provenance.
- NP723405.RA8AYGpI0kyrO-7lX5jIqYNwj4iBao7cWmAcKPlj2aj2c130_assertion wasDerivedFrom befree-20150227 NP723405.RA8AYGpI0kyrO-7lX5jIqYNwj4iBao7cWmAcKPlj2aj2c130_provenance.
- NP723405.RA8AYGpI0kyrO-7lX5jIqYNwj4iBao7cWmAcKPlj2aj2c130_assertion wasGeneratedBy ECO_0000203 NP723405.RA8AYGpI0kyrO-7lX5jIqYNwj4iBao7cWmAcKPlj2aj2c130_provenance.