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- NP710439.RA8p_-mfR8xzQLGgoc_dxI6LYvbLkP4xPD3evC2exZD34130_assertion type Assertion NP710439.RA8p_-mfR8xzQLGgoc_dxI6LYvbLkP4xPD3evC2exZD34130_head.
- NP710439.RA8p_-mfR8xzQLGgoc_dxI6LYvbLkP4xPD3evC2exZD34130_assertion wasGeneratedBy ECO_0000203 NP710439.RA8p_-mfR8xzQLGgoc_dxI6LYvbLkP4xPD3evC2exZD34130_provenance.
- NP710439.RA8p_-mfR8xzQLGgoc_dxI6LYvbLkP4xPD3evC2exZD34130_assertion wasDerivedFrom befree-2016 NP710439.RA8p_-mfR8xzQLGgoc_dxI6LYvbLkP4xPD3evC2exZD34130_provenance.
- NP710439.RA8p_-mfR8xzQLGgoc_dxI6LYvbLkP4xPD3evC2exZD34130_assertion SIO_000772 19097999 NP710439.RA8p_-mfR8xzQLGgoc_dxI6LYvbLkP4xPD3evC2exZD34130_provenance.
- NP710439.RA8p_-mfR8xzQLGgoc_dxI6LYvbLkP4xPD3evC2exZD34130_assertion evidence source_evidence_literature NP710439.RA8p_-mfR8xzQLGgoc_dxI6LYvbLkP4xPD3evC2exZD34130_provenance.
- NP710439.RA8p_-mfR8xzQLGgoc_dxI6LYvbLkP4xPD3evC2exZD34130_assertion description "[Fragile X syndrome is a common inherited cause of mental retardation that results from loss or mutation of the fragile X mental retardation protein (FMRP).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP710439.RA8p_-mfR8xzQLGgoc_dxI6LYvbLkP4xPD3evC2exZD34130_provenance.