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- NP947916.RABPxPj_NwbuenZYw_cTHlk66Xn7mavwZQ_Q7l7h0emkw130_assertion type Assertion NP947916.RABPxPj_NwbuenZYw_cTHlk66Xn7mavwZQ_Q7l7h0emkw130_head.
- NP947916.RABPxPj_NwbuenZYw_cTHlk66Xn7mavwZQ_Q7l7h0emkw130_assertion description "[In man, mutations in the NMD factor gene UPF3B, which disrupts a branch of the NMD pathway, cause various forms of intellectual disability (ID).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP947916.RABPxPj_NwbuenZYw_cTHlk66Xn7mavwZQ_Q7l7h0emkw130_provenance.
- NP947916.RABPxPj_NwbuenZYw_cTHlk66Xn7mavwZQ_Q7l7h0emkw130_assertion evidence source_evidence_literature NP947916.RABPxPj_NwbuenZYw_cTHlk66Xn7mavwZQ_Q7l7h0emkw130_provenance.
- NP947916.RABPxPj_NwbuenZYw_cTHlk66Xn7mavwZQ_Q7l7h0emkw130_assertion SIO_000772 22182939 NP947916.RABPxPj_NwbuenZYw_cTHlk66Xn7mavwZQ_Q7l7h0emkw130_provenance.
- NP947916.RABPxPj_NwbuenZYw_cTHlk66Xn7mavwZQ_Q7l7h0emkw130_assertion wasDerivedFrom befree-2016 NP947916.RABPxPj_NwbuenZYw_cTHlk66Xn7mavwZQ_Q7l7h0emkw130_provenance.
- NP947916.RABPxPj_NwbuenZYw_cTHlk66Xn7mavwZQ_Q7l7h0emkw130_assertion wasGeneratedBy ECO_0000203 NP947916.RABPxPj_NwbuenZYw_cTHlk66Xn7mavwZQ_Q7l7h0emkw130_provenance.