Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP674783.RAIVEjVzCmgx4kWQRZXb0j3PIEyPImUmEK1VMZjbjVgCM130_assertion> ?p ?o ?g. }
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- NP674783.RAIVEjVzCmgx4kWQRZXb0j3PIEyPImUmEK1VMZjbjVgCM130_assertion type Assertion NP674783.RAIVEjVzCmgx4kWQRZXb0j3PIEyPImUmEK1VMZjbjVgCM130_head.
- NP674783.RAIVEjVzCmgx4kWQRZXb0j3PIEyPImUmEK1VMZjbjVgCM130_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." NP674783.RAIVEjVzCmgx4kWQRZXb0j3PIEyPImUmEK1VMZjbjVgCM130_provenance.
- NP674783.RAIVEjVzCmgx4kWQRZXb0j3PIEyPImUmEK1VMZjbjVgCM130_assertion evidence source_evidence_literature NP674783.RAIVEjVzCmgx4kWQRZXb0j3PIEyPImUmEK1VMZjbjVgCM130_provenance.
- NP674783.RAIVEjVzCmgx4kWQRZXb0j3PIEyPImUmEK1VMZjbjVgCM130_assertion SIO_000772 18521840 NP674783.RAIVEjVzCmgx4kWQRZXb0j3PIEyPImUmEK1VMZjbjVgCM130_provenance.
- NP674783.RAIVEjVzCmgx4kWQRZXb0j3PIEyPImUmEK1VMZjbjVgCM130_assertion wasDerivedFrom befree-2016 NP674783.RAIVEjVzCmgx4kWQRZXb0j3PIEyPImUmEK1VMZjbjVgCM130_provenance.
- NP674783.RAIVEjVzCmgx4kWQRZXb0j3PIEyPImUmEK1VMZjbjVgCM130_assertion wasGeneratedBy ECO_0000203 NP674783.RAIVEjVzCmgx4kWQRZXb0j3PIEyPImUmEK1VMZjbjVgCM130_provenance.