Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP722934.RA1xIRsjKhcqhm1z_96dQdRbYaW_T6fBAmJNaquY_k_9A130_assertion> ?p ?o ?g. }
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- NP722934.RA1xIRsjKhcqhm1z_96dQdRbYaW_T6fBAmJNaquY_k_9A130_assertion type Assertion NP722934.RA1xIRsjKhcqhm1z_96dQdRbYaW_T6fBAmJNaquY_k_9A130_head.
- NP722934.RA1xIRsjKhcqhm1z_96dQdRbYaW_T6fBAmJNaquY_k_9A130_assertion description "[Chordin is a modifier of tbx1 for the craniofacial malformations of 22q11 deletion syndrome phenotypes in mouse.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP722934.RA1xIRsjKhcqhm1z_96dQdRbYaW_T6fBAmJNaquY_k_9A130_provenance.
- NP722934.RA1xIRsjKhcqhm1z_96dQdRbYaW_T6fBAmJNaquY_k_9A130_assertion evidence source_evidence_literature NP722934.RA1xIRsjKhcqhm1z_96dQdRbYaW_T6fBAmJNaquY_k_9A130_provenance.
- NP722934.RA1xIRsjKhcqhm1z_96dQdRbYaW_T6fBAmJNaquY_k_9A130_assertion SIO_000772 19247433 NP722934.RA1xIRsjKhcqhm1z_96dQdRbYaW_T6fBAmJNaquY_k_9A130_provenance.
- NP722934.RA1xIRsjKhcqhm1z_96dQdRbYaW_T6fBAmJNaquY_k_9A130_assertion wasDerivedFrom befree-2016 NP722934.RA1xIRsjKhcqhm1z_96dQdRbYaW_T6fBAmJNaquY_k_9A130_provenance.
- NP722934.RA1xIRsjKhcqhm1z_96dQdRbYaW_T6fBAmJNaquY_k_9A130_assertion wasGeneratedBy ECO_0000203 NP722934.RA1xIRsjKhcqhm1z_96dQdRbYaW_T6fBAmJNaquY_k_9A130_provenance.