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- NP715769.RACkghHpRykfllmk_2F2p1nL50PeI_9wEbIWU-HCpUrX4130_assertion type Assertion NP715769.RACkghHpRykfllmk_2F2p1nL50PeI_9wEbIWU-HCpUrX4130_head.
- NP715769.RACkghHpRykfllmk_2F2p1nL50PeI_9wEbIWU-HCpUrX4130_assertion description "[A loss-of-function mutation in the FMR1 gene leads to subtle changes in neural development and subsequent mental impairment characteristic of FX.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP715769.RACkghHpRykfllmk_2F2p1nL50PeI_9wEbIWU-HCpUrX4130_provenance.
- NP715769.RACkghHpRykfllmk_2F2p1nL50PeI_9wEbIWU-HCpUrX4130_assertion evidence source_evidence_literature NP715769.RACkghHpRykfllmk_2F2p1nL50PeI_9wEbIWU-HCpUrX4130_provenance.
- NP715769.RACkghHpRykfllmk_2F2p1nL50PeI_9wEbIWU-HCpUrX4130_assertion SIO_000772 18225979 NP715769.RACkghHpRykfllmk_2F2p1nL50PeI_9wEbIWU-HCpUrX4130_provenance.
- NP715769.RACkghHpRykfllmk_2F2p1nL50PeI_9wEbIWU-HCpUrX4130_assertion wasDerivedFrom befree-20140225 NP715769.RACkghHpRykfllmk_2F2p1nL50PeI_9wEbIWU-HCpUrX4130_provenance.
- NP715769.RACkghHpRykfllmk_2F2p1nL50PeI_9wEbIWU-HCpUrX4130_assertion wasGeneratedBy ECO_0000203 NP715769.RACkghHpRykfllmk_2F2p1nL50PeI_9wEbIWU-HCpUrX4130_provenance.