Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP503100.RAZmZfkFdyVVxaRJrCXcvGkvWCQD6IfjbbEr4w9urCdHk130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP503100.RAZmZfkFdyVVxaRJrCXcvGkvWCQD6IfjbbEr4w9urCdHk130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP503100.RAZmZfkFdyVVxaRJrCXcvGkvWCQD6IfjbbEr4w9urCdHk130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP503100.RAZmZfkFdyVVxaRJrCXcvGkvWCQD6IfjbbEr4w9urCdHk130_provenance.
- NP503100.RAZmZfkFdyVVxaRJrCXcvGkvWCQD6IfjbbEr4w9urCdHk130_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." NP503100.RAZmZfkFdyVVxaRJrCXcvGkvWCQD6IfjbbEr4w9urCdHk130_provenance.
- NP503100.RAZmZfkFdyVVxaRJrCXcvGkvWCQD6IfjbbEr4w9urCdHk130_assertion evidence source_evidence_literature NP503100.RAZmZfkFdyVVxaRJrCXcvGkvWCQD6IfjbbEr4w9urCdHk130_provenance.
- NP503100.RAZmZfkFdyVVxaRJrCXcvGkvWCQD6IfjbbEr4w9urCdHk130_assertion SIO_000772 16004559 NP503100.RAZmZfkFdyVVxaRJrCXcvGkvWCQD6IfjbbEr4w9urCdHk130_provenance.
- NP503100.RAZmZfkFdyVVxaRJrCXcvGkvWCQD6IfjbbEr4w9urCdHk130_assertion wasDerivedFrom befree-2016 NP503100.RAZmZfkFdyVVxaRJrCXcvGkvWCQD6IfjbbEr4w9urCdHk130_provenance.
- NP503100.RAZmZfkFdyVVxaRJrCXcvGkvWCQD6IfjbbEr4w9urCdHk130_assertion wasGeneratedBy ECO_0000203 NP503100.RAZmZfkFdyVVxaRJrCXcvGkvWCQD6IfjbbEr4w9urCdHk130_provenance.
- befree-2016 importedOn "2016-02-19" NP503100.RAZmZfkFdyVVxaRJrCXcvGkvWCQD6IfjbbEr4w9urCdHk130_provenance.