Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP434882.RA1HdAfADslP8X6nmV_SF_XJfqi-u1pT_iGs_XxWcIq1Y130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP434882.RA1HdAfADslP8X6nmV_SF_XJfqi-u1pT_iGs_XxWcIq1Y130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP434882.RA1HdAfADslP8X6nmV_SF_XJfqi-u1pT_iGs_XxWcIq1Y130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP434882.RA1HdAfADslP8X6nmV_SF_XJfqi-u1pT_iGs_XxWcIq1Y130_provenance.
- NP434882.RA1HdAfADslP8X6nmV_SF_XJfqi-u1pT_iGs_XxWcIq1Y130_assertion description "[Xq27 FRAXA locus is a strong candidate for dyslexia: evidence from a genome-wide scan in French families.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP434882.RA1HdAfADslP8X6nmV_SF_XJfqi-u1pT_iGs_XxWcIq1Y130_provenance.
- NP434882.RA1HdAfADslP8X6nmV_SF_XJfqi-u1pT_iGs_XxWcIq1Y130_assertion evidence source_evidence_literature NP434882.RA1HdAfADslP8X6nmV_SF_XJfqi-u1pT_iGs_XxWcIq1Y130_provenance.
- NP434882.RA1HdAfADslP8X6nmV_SF_XJfqi-u1pT_iGs_XxWcIq1Y130_assertion SIO_000772 23307483 NP434882.RA1HdAfADslP8X6nmV_SF_XJfqi-u1pT_iGs_XxWcIq1Y130_provenance.
- NP434882.RA1HdAfADslP8X6nmV_SF_XJfqi-u1pT_iGs_XxWcIq1Y130_assertion wasDerivedFrom befree-20140225 NP434882.RA1HdAfADslP8X6nmV_SF_XJfqi-u1pT_iGs_XxWcIq1Y130_provenance.
- NP434882.RA1HdAfADslP8X6nmV_SF_XJfqi-u1pT_iGs_XxWcIq1Y130_assertion wasGeneratedBy ECO_0000203 NP434882.RA1HdAfADslP8X6nmV_SF_XJfqi-u1pT_iGs_XxWcIq1Y130_provenance.
- befree-20140225 importedOn "2014-02-25" NP434882.RA1HdAfADslP8X6nmV_SF_XJfqi-u1pT_iGs_XxWcIq1Y130_provenance.