Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP463425.RAmlNih7yA6Kbhwi4ymJg8HZhViI9TCukr7Oy-RgrmOr0130_assertion> ?p ?o ?g. }
Showing items 1 to 6 of
6
with 100 items per page.
- NP463425.RAmlNih7yA6Kbhwi4ymJg8HZhViI9TCukr7Oy-RgrmOr0130_assertion type Assertion NP463425.RAmlNih7yA6Kbhwi4ymJg8HZhViI9TCukr7Oy-RgrmOr0130_head.
- NP463425.RAmlNih7yA6Kbhwi4ymJg8HZhViI9TCukr7Oy-RgrmOr0130_assertion description "[DYX1C1: was recently identified as a candidate gene for developmental dyslexia, which is characterized by an unexpected difficulty in learning to read and write despite adequate intelligence, motivation, and education.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP463425.RAmlNih7yA6Kbhwi4ymJg8HZhViI9TCukr7Oy-RgrmOr0130_provenance.
- NP463425.RAmlNih7yA6Kbhwi4ymJg8HZhViI9TCukr7Oy-RgrmOr0130_assertion evidence source_evidence_literature NP463425.RAmlNih7yA6Kbhwi4ymJg8HZhViI9TCukr7Oy-RgrmOr0130_provenance.
- NP463425.RAmlNih7yA6Kbhwi4ymJg8HZhViI9TCukr7Oy-RgrmOr0130_assertion SIO_000772 15470369 NP463425.RAmlNih7yA6Kbhwi4ymJg8HZhViI9TCukr7Oy-RgrmOr0130_provenance.
- NP463425.RAmlNih7yA6Kbhwi4ymJg8HZhViI9TCukr7Oy-RgrmOr0130_assertion wasDerivedFrom befree-2016 NP463425.RAmlNih7yA6Kbhwi4ymJg8HZhViI9TCukr7Oy-RgrmOr0130_provenance.
- NP463425.RAmlNih7yA6Kbhwi4ymJg8HZhViI9TCukr7Oy-RgrmOr0130_assertion wasGeneratedBy ECO_0000203 NP463425.RAmlNih7yA6Kbhwi4ymJg8HZhViI9TCukr7Oy-RgrmOr0130_provenance.