Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP831130.RAgxGTL58GneB3y3byn6iVsu0Qt3XG0FAe0t9-S4WlBZU130_assertion> ?p ?o ?g. }
Showing items 1 to 6 of
6
with 100 items per page.
- NP831130.RAgxGTL58GneB3y3byn6iVsu0Qt3XG0FAe0t9-S4WlBZU130_assertion type Assertion NP831130.RAgxGTL58GneB3y3byn6iVsu0Qt3XG0FAe0t9-S4WlBZU130_head.
- NP831130.RAgxGTL58GneB3y3byn6iVsu0Qt3XG0FAe0t9-S4WlBZU130_assertion description "[ZFHX1B mutations cause a complex developmental phenotype characterized by severe mental retardation (MR) and multiple congenital defects.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP831130.RAgxGTL58GneB3y3byn6iVsu0Qt3XG0FAe0t9-S4WlBZU130_provenance.
- NP831130.RAgxGTL58GneB3y3byn6iVsu0Qt3XG0FAe0t9-S4WlBZU130_assertion evidence source_evidence_literature NP831130.RAgxGTL58GneB3y3byn6iVsu0Qt3XG0FAe0t9-S4WlBZU130_provenance.
- NP831130.RAgxGTL58GneB3y3byn6iVsu0Qt3XG0FAe0t9-S4WlBZU130_assertion SIO_000772 15006694 NP831130.RAgxGTL58GneB3y3byn6iVsu0Qt3XG0FAe0t9-S4WlBZU130_provenance.
- NP831130.RAgxGTL58GneB3y3byn6iVsu0Qt3XG0FAe0t9-S4WlBZU130_assertion wasDerivedFrom befree-20150227 NP831130.RAgxGTL58GneB3y3byn6iVsu0Qt3XG0FAe0t9-S4WlBZU130_provenance.
- NP831130.RAgxGTL58GneB3y3byn6iVsu0Qt3XG0FAe0t9-S4WlBZU130_assertion wasGeneratedBy ECO_0000203 NP831130.RAgxGTL58GneB3y3byn6iVsu0Qt3XG0FAe0t9-S4WlBZU130_provenance.