Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP463425.RAmlNih7yA6Kbhwi4ymJg8HZhViI9TCukr7Oy-RgrmOr0130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP463425.RAmlNih7yA6Kbhwi4ymJg8HZhViI9TCukr7Oy-RgrmOr0130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP463425.RAmlNih7yA6Kbhwi4ymJg8HZhViI9TCukr7Oy-RgrmOr0130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP463425.RAmlNih7yA6Kbhwi4ymJg8HZhViI9TCukr7Oy-RgrmOr0130_provenance.
- 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.
- befree-2016 importedOn "2016-02-19" NP463425.RAmlNih7yA6Kbhwi4ymJg8HZhViI9TCukr7Oy-RgrmOr0130_provenance.