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- source_evidence_literature type ECO_0000212 NP612512.RAPspVmyGRLJVxEG3MahetSCPZjrtp5IyJppltvNAKDQY130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP612512.RAPspVmyGRLJVxEG3MahetSCPZjrtp5IyJppltvNAKDQY130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP612512.RAPspVmyGRLJVxEG3MahetSCPZjrtp5IyJppltvNAKDQY130_provenance.
- NP612512.RAPspVmyGRLJVxEG3MahetSCPZjrtp5IyJppltvNAKDQY130_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." NP612512.RAPspVmyGRLJVxEG3MahetSCPZjrtp5IyJppltvNAKDQY130_provenance.
- NP612512.RAPspVmyGRLJVxEG3MahetSCPZjrtp5IyJppltvNAKDQY130_assertion evidence source_evidence_literature NP612512.RAPspVmyGRLJVxEG3MahetSCPZjrtp5IyJppltvNAKDQY130_provenance.
- NP612512.RAPspVmyGRLJVxEG3MahetSCPZjrtp5IyJppltvNAKDQY130_assertion SIO_000772 18521840 NP612512.RAPspVmyGRLJVxEG3MahetSCPZjrtp5IyJppltvNAKDQY130_provenance.
- NP612512.RAPspVmyGRLJVxEG3MahetSCPZjrtp5IyJppltvNAKDQY130_assertion wasDerivedFrom befree-20150227 NP612512.RAPspVmyGRLJVxEG3MahetSCPZjrtp5IyJppltvNAKDQY130_provenance.
- NP612512.RAPspVmyGRLJVxEG3MahetSCPZjrtp5IyJppltvNAKDQY130_assertion wasGeneratedBy ECO_0000203 NP612512.RAPspVmyGRLJVxEG3MahetSCPZjrtp5IyJppltvNAKDQY130_provenance.
- befree-20150227 importedOn "2015-02-27" NP612512.RAPspVmyGRLJVxEG3MahetSCPZjrtp5IyJppltvNAKDQY130_provenance.