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- NP766573.RA3b-jaKmGu-Egj0Bz7PlqIeWvgEC5PLnJgDub-e7YIeY130_assertion type Assertion NP766573.RA3b-jaKmGu-Egj0Bz7PlqIeWvgEC5PLnJgDub-e7YIeY130_head.
- NP766573.RA3b-jaKmGu-Egj0Bz7PlqIeWvgEC5PLnJgDub-e7YIeY130_assertion description "[This mechanism is entirely different from the mechanism giving rise to fragile X syndrome, which is due to transcriptional silencing and consequent loss of FMR1 protein.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP766573.RA3b-jaKmGu-Egj0Bz7PlqIeWvgEC5PLnJgDub-e7YIeY130_provenance.
- NP766573.RA3b-jaKmGu-Egj0Bz7PlqIeWvgEC5PLnJgDub-e7YIeY130_assertion evidence source_evidence_literature NP766573.RA3b-jaKmGu-Egj0Bz7PlqIeWvgEC5PLnJgDub-e7YIeY130_provenance.
- NP766573.RA3b-jaKmGu-Egj0Bz7PlqIeWvgEC5PLnJgDub-e7YIeY130_assertion SIO_000772 19794313 NP766573.RA3b-jaKmGu-Egj0Bz7PlqIeWvgEC5PLnJgDub-e7YIeY130_provenance.
- NP766573.RA3b-jaKmGu-Egj0Bz7PlqIeWvgEC5PLnJgDub-e7YIeY130_assertion wasDerivedFrom befree-2016 NP766573.RA3b-jaKmGu-Egj0Bz7PlqIeWvgEC5PLnJgDub-e7YIeY130_provenance.
- NP766573.RA3b-jaKmGu-Egj0Bz7PlqIeWvgEC5PLnJgDub-e7YIeY130_assertion wasGeneratedBy ECO_0000203 NP766573.RA3b-jaKmGu-Egj0Bz7PlqIeWvgEC5PLnJgDub-e7YIeY130_provenance.