Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP556993.RAAgt5m3Ta1dKzIiu-WnkutFfiyTJJaTSxTeOA3lFuO6c130_assertion> ?p ?o ?g. }
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- NP556993.RAAgt5m3Ta1dKzIiu-WnkutFfiyTJJaTSxTeOA3lFuO6c130_assertion type Assertion NP556993.RAAgt5m3Ta1dKzIiu-WnkutFfiyTJJaTSxTeOA3lFuO6c130_head.
- NP556993.RAAgt5m3Ta1dKzIiu-WnkutFfiyTJJaTSxTeOA3lFuO6c130_assertion description "[Mutations of ZFHX1B are frequently associated with other congenital anomalies, including congenital heart disease, hypospadias, renal tract anomalies, and agenesis of the corpus callosum (ACC).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP556993.RAAgt5m3Ta1dKzIiu-WnkutFfiyTJJaTSxTeOA3lFuO6c130_provenance.
- NP556993.RAAgt5m3Ta1dKzIiu-WnkutFfiyTJJaTSxTeOA3lFuO6c130_assertion evidence source_evidence_literature NP556993.RAAgt5m3Ta1dKzIiu-WnkutFfiyTJJaTSxTeOA3lFuO6c130_provenance.
- NP556993.RAAgt5m3Ta1dKzIiu-WnkutFfiyTJJaTSxTeOA3lFuO6c130_assertion SIO_000772 12784289 NP556993.RAAgt5m3Ta1dKzIiu-WnkutFfiyTJJaTSxTeOA3lFuO6c130_provenance.
- NP556993.RAAgt5m3Ta1dKzIiu-WnkutFfiyTJJaTSxTeOA3lFuO6c130_assertion wasDerivedFrom befree-20140225 NP556993.RAAgt5m3Ta1dKzIiu-WnkutFfiyTJJaTSxTeOA3lFuO6c130_provenance.
- NP556993.RAAgt5m3Ta1dKzIiu-WnkutFfiyTJJaTSxTeOA3lFuO6c130_assertion wasGeneratedBy ECO_0000203 NP556993.RAAgt5m3Ta1dKzIiu-WnkutFfiyTJJaTSxTeOA3lFuO6c130_provenance.