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- NP674781.RAaL8MSNbH5XaeH-B246mh7Yry41alTRTHYXxgW6GNUSc130_assertion type Assertion NP674781.RAaL8MSNbH5XaeH-B246mh7Yry41alTRTHYXxgW6GNUSc130_head.
- NP674781.RAaL8MSNbH5XaeH-B246mh7Yry41alTRTHYXxgW6GNUSc130_assertion description "[In this article, we report the identification of four new dyslexia candidate genes (PCNT, DIP2A, S100B, and PRMT2) on chromosome region 21q22.3 by FISH and SNP microarray analyses of a very small deletion in this region, which cosegregates with dyslexia in a father and his three sons.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP674781.RAaL8MSNbH5XaeH-B246mh7Yry41alTRTHYXxgW6GNUSc130_provenance.
- NP674781.RAaL8MSNbH5XaeH-B246mh7Yry41alTRTHYXxgW6GNUSc130_assertion evidence source_evidence_literature NP674781.RAaL8MSNbH5XaeH-B246mh7Yry41alTRTHYXxgW6GNUSc130_provenance.
- NP674781.RAaL8MSNbH5XaeH-B246mh7Yry41alTRTHYXxgW6GNUSc130_assertion SIO_000772 18521840 NP674781.RAaL8MSNbH5XaeH-B246mh7Yry41alTRTHYXxgW6GNUSc130_provenance.
- NP674781.RAaL8MSNbH5XaeH-B246mh7Yry41alTRTHYXxgW6GNUSc130_assertion wasDerivedFrom befree-2016 NP674781.RAaL8MSNbH5XaeH-B246mh7Yry41alTRTHYXxgW6GNUSc130_provenance.
- NP674781.RAaL8MSNbH5XaeH-B246mh7Yry41alTRTHYXxgW6GNUSc130_assertion wasGeneratedBy ECO_0000203 NP674781.RAaL8MSNbH5XaeH-B246mh7Yry41alTRTHYXxgW6GNUSc130_provenance.