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- NP26289.RA_EQHe112cM5W8TlNTyxTj265jww7IZoY9Qk-Y4SET5c130_assertion type Assertion NP26289.RA_EQHe112cM5W8TlNTyxTj265jww7IZoY9Qk-Y4SET5c130_head.
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- NP26289.RA_EQHe112cM5W8TlNTyxTj265jww7IZoY9Qk-Y4SET5c130_assertion wasDerivedFrom ctd_human-2016 NP26289.RA_EQHe112cM5W8TlNTyxTj265jww7IZoY9Qk-Y4SET5c130_provenance.
- NP26289.RA_EQHe112cM5W8TlNTyxTj265jww7IZoY9Qk-Y4SET5c130_assertion SIO_000772 20531469 NP26289.RA_EQHe112cM5W8TlNTyxTj265jww7IZoY9Qk-Y4SET5c130_provenance.
- NP26289.RA_EQHe112cM5W8TlNTyxTj265jww7IZoY9Qk-Y4SET5c130_assertion evidence source_evidence_curated NP26289.RA_EQHe112cM5W8TlNTyxTj265jww7IZoY9Qk-Y4SET5c130_provenance.
- NP26289.RA_EQHe112cM5W8TlNTyxTj265jww7IZoY9Qk-Y4SET5c130_assertion description "[Functional impact of global rare copy number variation in autism spectrum disorders.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP26289.RA_EQHe112cM5W8TlNTyxTj265jww7IZoY9Qk-Y4SET5c130_provenance.