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- NP723307.RAwCPKR1ZtxBx1w7Hw3x7_b6s6W3pJ47CZq9A8y1VIjjs130_assertion type Assertion NP723307.RAwCPKR1ZtxBx1w7Hw3x7_b6s6W3pJ47CZq9A8y1VIjjs130_head.
- NP723307.RAwCPKR1ZtxBx1w7Hw3x7_b6s6W3pJ47CZq9A8y1VIjjs130_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." NP723307.RAwCPKR1ZtxBx1w7Hw3x7_b6s6W3pJ47CZq9A8y1VIjjs130_provenance.
- NP723307.RAwCPKR1ZtxBx1w7Hw3x7_b6s6W3pJ47CZq9A8y1VIjjs130_assertion evidence source_evidence_literature NP723307.RAwCPKR1ZtxBx1w7Hw3x7_b6s6W3pJ47CZq9A8y1VIjjs130_provenance.
- NP723307.RAwCPKR1ZtxBx1w7Hw3x7_b6s6W3pJ47CZq9A8y1VIjjs130_assertion SIO_000772 22893440 NP723307.RAwCPKR1ZtxBx1w7Hw3x7_b6s6W3pJ47CZq9A8y1VIjjs130_provenance.
- NP723307.RAwCPKR1ZtxBx1w7Hw3x7_b6s6W3pJ47CZq9A8y1VIjjs130_assertion wasDerivedFrom befree-20150227 NP723307.RAwCPKR1ZtxBx1w7Hw3x7_b6s6W3pJ47CZq9A8y1VIjjs130_provenance.
- NP723307.RAwCPKR1ZtxBx1w7Hw3x7_b6s6W3pJ47CZq9A8y1VIjjs130_assertion wasGeneratedBy ECO_0000203 NP723307.RAwCPKR1ZtxBx1w7Hw3x7_b6s6W3pJ47CZq9A8y1VIjjs130_provenance.