Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP301130.RAQW9Rol8r08AUwOr9WkIxL6wF5NyIe0vCQThM0nVoCQc130_assertion> ?p ?o ?g. }
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- NP301130.RAQW9Rol8r08AUwOr9WkIxL6wF5NyIe0vCQThM0nVoCQc130_assertion type Assertion NP301130.RAQW9Rol8r08AUwOr9WkIxL6wF5NyIe0vCQThM0nVoCQc130_head.
- 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.
- NP301130.RAQW9Rol8r08AUwOr9WkIxL6wF5NyIe0vCQThM0nVoCQc130_assertion evidence source_evidence_literature NP301130.RAQW9Rol8r08AUwOr9WkIxL6wF5NyIe0vCQThM0nVoCQc130_provenance.
- NP301130.RAQW9Rol8r08AUwOr9WkIxL6wF5NyIe0vCQThM0nVoCQc130_assertion SIO_000772 19901951 NP301130.RAQW9Rol8r08AUwOr9WkIxL6wF5NyIe0vCQThM0nVoCQc130_provenance.
- NP301130.RAQW9Rol8r08AUwOr9WkIxL6wF5NyIe0vCQThM0nVoCQc130_assertion wasDerivedFrom befree-20140225 NP301130.RAQW9Rol8r08AUwOr9WkIxL6wF5NyIe0vCQThM0nVoCQc130_provenance.
- NP301130.RAQW9Rol8r08AUwOr9WkIxL6wF5NyIe0vCQThM0nVoCQc130_assertion wasGeneratedBy ECO_0000203 NP301130.RAQW9Rol8r08AUwOr9WkIxL6wF5NyIe0vCQThM0nVoCQc130_provenance.