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- source_evidence_literature type ECO_0000212 NP1046103.RALnTrRorN8-sCbWt4OLgCmNWOI_QwIxkE-19RElB1djI130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP1046103.RALnTrRorN8-sCbWt4OLgCmNWOI_QwIxkE-19RElB1djI130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP1046103.RALnTrRorN8-sCbWt4OLgCmNWOI_QwIxkE-19RElB1djI130_provenance.
- NP1046103.RALnTrRorN8-sCbWt4OLgCmNWOI_QwIxkE-19RElB1djI130_assertion description "[Dyslexia susceptibility 1 candidate gene 1 (DYX1C1) on chromosome 15q21 was originally proposed as a candidate gene with two potentially functional polymorphisms at the -3G/A and 1249G/T positions showing association with RD.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1046103.RALnTrRorN8-sCbWt4OLgCmNWOI_QwIxkE-19RElB1djI130_provenance.
- NP1046103.RALnTrRorN8-sCbWt4OLgCmNWOI_QwIxkE-19RElB1djI130_assertion evidence source_evidence_literature NP1046103.RALnTrRorN8-sCbWt4OLgCmNWOI_QwIxkE-19RElB1djI130_provenance.
- NP1046103.RALnTrRorN8-sCbWt4OLgCmNWOI_QwIxkE-19RElB1djI130_assertion SIO_000772 23341075 NP1046103.RALnTrRorN8-sCbWt4OLgCmNWOI_QwIxkE-19RElB1djI130_provenance.
- NP1046103.RALnTrRorN8-sCbWt4OLgCmNWOI_QwIxkE-19RElB1djI130_assertion wasDerivedFrom befree-2016 NP1046103.RALnTrRorN8-sCbWt4OLgCmNWOI_QwIxkE-19RElB1djI130_provenance.
- NP1046103.RALnTrRorN8-sCbWt4OLgCmNWOI_QwIxkE-19RElB1djI130_assertion wasGeneratedBy ECO_0000203 NP1046103.RALnTrRorN8-sCbWt4OLgCmNWOI_QwIxkE-19RElB1djI130_provenance.
- befree-2016 importedOn "2016-02-19" NP1046103.RALnTrRorN8-sCbWt4OLgCmNWOI_QwIxkE-19RElB1djI130_provenance.