Matches in Nanopublications for { ?s ?p "[Missense mutation rs17819126 is a potential functional basis for the association of DYX1C1 with dyslexia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ?g. }
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- NP301130.RAQW9Rol8r08AUwOr9WkIxL6wF5NyIe0vCQThM0nVoCQc130_assertion description "[Missense mutation rs17819126 is a potential functional basis for the association of DYX1C1 with dyslexia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP301130.RAQW9Rol8r08AUwOr9WkIxL6wF5NyIe0vCQThM0nVoCQc130_provenance.