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- source_evidence_literature type ECO_0000212 NP679962.RAxxRE8fFz1yOXwQVVzpTxxdI00E_mrTmBgnRSHw5Ogaw130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP679962.RAxxRE8fFz1yOXwQVVzpTxxdI00E_mrTmBgnRSHw5Ogaw130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP679962.RAxxRE8fFz1yOXwQVVzpTxxdI00E_mrTmBgnRSHw5Ogaw130_provenance.
- NP679962.RAxxRE8fFz1yOXwQVVzpTxxdI00E_mrTmBgnRSHw5Ogaw130_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." NP679962.RAxxRE8fFz1yOXwQVVzpTxxdI00E_mrTmBgnRSHw5Ogaw130_provenance.
- NP679962.RAxxRE8fFz1yOXwQVVzpTxxdI00E_mrTmBgnRSHw5Ogaw130_assertion evidence source_evidence_literature NP679962.RAxxRE8fFz1yOXwQVVzpTxxdI00E_mrTmBgnRSHw5Ogaw130_provenance.
- NP679962.RAxxRE8fFz1yOXwQVVzpTxxdI00E_mrTmBgnRSHw5Ogaw130_assertion SIO_000772 18521840 NP679962.RAxxRE8fFz1yOXwQVVzpTxxdI00E_mrTmBgnRSHw5Ogaw130_provenance.
- NP679962.RAxxRE8fFz1yOXwQVVzpTxxdI00E_mrTmBgnRSHw5Ogaw130_assertion wasDerivedFrom befree-20150227 NP679962.RAxxRE8fFz1yOXwQVVzpTxxdI00E_mrTmBgnRSHw5Ogaw130_provenance.
- NP679962.RAxxRE8fFz1yOXwQVVzpTxxdI00E_mrTmBgnRSHw5Ogaw130_assertion wasGeneratedBy ECO_0000203 NP679962.RAxxRE8fFz1yOXwQVVzpTxxdI00E_mrTmBgnRSHw5Ogaw130_provenance.
- befree-20150227 importedOn "2015-02-27" NP679962.RAxxRE8fFz1yOXwQVVzpTxxdI00E_mrTmBgnRSHw5Ogaw130_provenance.