Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP674781.RAaL8MSNbH5XaeH-B246mh7Yry41alTRTHYXxgW6GNUSc130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP674781.RAaL8MSNbH5XaeH-B246mh7Yry41alTRTHYXxgW6GNUSc130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP674781.RAaL8MSNbH5XaeH-B246mh7Yry41alTRTHYXxgW6GNUSc130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP674781.RAaL8MSNbH5XaeH-B246mh7Yry41alTRTHYXxgW6GNUSc130_provenance.
- 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.
- befree-2016 importedOn "2016-02-19" NP674781.RAaL8MSNbH5XaeH-B246mh7Yry41alTRTHYXxgW6GNUSc130_provenance.