Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP722937.RA7IdFjQMUrWCX6OzvRsWcnHlMaOUYdYZhMHi5j14pU20130_assertion> ?p ?o ?g. }
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- NP722937.RA7IdFjQMUrWCX6OzvRsWcnHlMaOUYdYZhMHi5j14pU20130_assertion type Assertion NP722937.RA7IdFjQMUrWCX6OzvRsWcnHlMaOUYdYZhMHi5j14pU20130_head.
- NP722937.RA7IdFjQMUrWCX6OzvRsWcnHlMaOUYdYZhMHi5j14pU20130_assertion description "[Thus, chordin is a modifier for the craniofacial anomalies of Tbx1 mutations, demonstrating the existence of a second-site modifier for a specific subset of the phenotypes associated with 22q11DS.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP722937.RA7IdFjQMUrWCX6OzvRsWcnHlMaOUYdYZhMHi5j14pU20130_provenance.
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- NP722937.RA7IdFjQMUrWCX6OzvRsWcnHlMaOUYdYZhMHi5j14pU20130_assertion wasDerivedFrom befree-2016 NP722937.RA7IdFjQMUrWCX6OzvRsWcnHlMaOUYdYZhMHi5j14pU20130_provenance.
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