Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP705738.RA739Tq2IXAfX8g1pRI6sp7XMznoHwDxvDeL-7J8Ujdu8130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP705738.RA739Tq2IXAfX8g1pRI6sp7XMznoHwDxvDeL-7J8Ujdu8130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP705738.RA739Tq2IXAfX8g1pRI6sp7XMznoHwDxvDeL-7J8Ujdu8130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP705738.RA739Tq2IXAfX8g1pRI6sp7XMznoHwDxvDeL-7J8Ujdu8130_provenance.
- NP705738.RA739Tq2IXAfX8g1pRI6sp7XMznoHwDxvDeL-7J8Ujdu8130_assertion description "[In contrast, patients with the TTC/TTC, TTC/CGT, TTC/TGT, CGT/CGT and TGT/CGT haplotype combinations were more likely to be seizure-free (all p-values<0.0001 except CGT/CGT [p=0.0063]).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP705738.RA739Tq2IXAfX8g1pRI6sp7XMznoHwDxvDeL-7J8Ujdu8130_provenance.
- NP705738.RA739Tq2IXAfX8g1pRI6sp7XMznoHwDxvDeL-7J8Ujdu8130_assertion evidence source_evidence_literature NP705738.RA739Tq2IXAfX8g1pRI6sp7XMznoHwDxvDeL-7J8Ujdu8130_provenance.
- NP705738.RA739Tq2IXAfX8g1pRI6sp7XMznoHwDxvDeL-7J8Ujdu8130_assertion SIO_000772 16004559 NP705738.RA739Tq2IXAfX8g1pRI6sp7XMznoHwDxvDeL-7J8Ujdu8130_provenance.
- NP705738.RA739Tq2IXAfX8g1pRI6sp7XMznoHwDxvDeL-7J8Ujdu8130_assertion wasDerivedFrom befree-20140225 NP705738.RA739Tq2IXAfX8g1pRI6sp7XMznoHwDxvDeL-7J8Ujdu8130_provenance.
- NP705738.RA739Tq2IXAfX8g1pRI6sp7XMznoHwDxvDeL-7J8Ujdu8130_assertion wasGeneratedBy ECO_0000203 NP705738.RA739Tq2IXAfX8g1pRI6sp7XMznoHwDxvDeL-7J8Ujdu8130_provenance.
- befree-20140225 importedOn "2014-02-25" NP705738.RA739Tq2IXAfX8g1pRI6sp7XMznoHwDxvDeL-7J8Ujdu8130_provenance.