Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP652198.RABF1Jzz9tSrgTHQJrA_v3Ej_yuPCANQNfHfEwfCfoKDg130_assertion> ?p ?o ?g. }
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- NP652198.RABF1Jzz9tSrgTHQJrA_v3Ej_yuPCANQNfHfEwfCfoKDg130_assertion type Assertion NP652198.RABF1Jzz9tSrgTHQJrA_v3Ej_yuPCANQNfHfEwfCfoKDg130_head.
- NP652198.RABF1Jzz9tSrgTHQJrA_v3Ej_yuPCANQNfHfEwfCfoKDg130_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." NP652198.RABF1Jzz9tSrgTHQJrA_v3Ej_yuPCANQNfHfEwfCfoKDg130_provenance.
- NP652198.RABF1Jzz9tSrgTHQJrA_v3Ej_yuPCANQNfHfEwfCfoKDg130_assertion evidence source_evidence_literature NP652198.RABF1Jzz9tSrgTHQJrA_v3Ej_yuPCANQNfHfEwfCfoKDg130_provenance.
- NP652198.RABF1Jzz9tSrgTHQJrA_v3Ej_yuPCANQNfHfEwfCfoKDg130_assertion SIO_000772 18225979 NP652198.RABF1Jzz9tSrgTHQJrA_v3Ej_yuPCANQNfHfEwfCfoKDg130_provenance.
- NP652198.RABF1Jzz9tSrgTHQJrA_v3Ej_yuPCANQNfHfEwfCfoKDg130_assertion wasDerivedFrom befree-2016 NP652198.RABF1Jzz9tSrgTHQJrA_v3Ej_yuPCANQNfHfEwfCfoKDg130_provenance.
- NP652198.RABF1Jzz9tSrgTHQJrA_v3Ej_yuPCANQNfHfEwfCfoKDg130_assertion wasGeneratedBy ECO_0000203 NP652198.RABF1Jzz9tSrgTHQJrA_v3Ej_yuPCANQNfHfEwfCfoKDg130_provenance.