Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP724399.RAxEScofSCjh29k3v5SvyFj5C3VViNvGP8QDlM7SHn3BM130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP724399.RAxEScofSCjh29k3v5SvyFj5C3VViNvGP8QDlM7SHn3BM130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP724399.RAxEScofSCjh29k3v5SvyFj5C3VViNvGP8QDlM7SHn3BM130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP724399.RAxEScofSCjh29k3v5SvyFj5C3VViNvGP8QDlM7SHn3BM130_provenance.
- NP724399.RAxEScofSCjh29k3v5SvyFj5C3VViNvGP8QDlM7SHn3BM130_assertion description "[To assess the genetic association of transcription factor 4 (TCF4) intronic polymorphisms and CTG18.1 allele in individuals with Fuchs' endothelial corneal dystrophy (FECD) individuals from a sample Indian population.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP724399.RAxEScofSCjh29k3v5SvyFj5C3VViNvGP8QDlM7SHn3BM130_provenance.
- NP724399.RAxEScofSCjh29k3v5SvyFj5C3VViNvGP8QDlM7SHn3BM130_assertion evidence source_evidence_literature NP724399.RAxEScofSCjh29k3v5SvyFj5C3VViNvGP8QDlM7SHn3BM130_provenance.
- NP724399.RAxEScofSCjh29k3v5SvyFj5C3VViNvGP8QDlM7SHn3BM130_assertion SIO_000772 25342617 NP724399.RAxEScofSCjh29k3v5SvyFj5C3VViNvGP8QDlM7SHn3BM130_provenance.
- NP724399.RAxEScofSCjh29k3v5SvyFj5C3VViNvGP8QDlM7SHn3BM130_assertion wasDerivedFrom befree-20150227 NP724399.RAxEScofSCjh29k3v5SvyFj5C3VViNvGP8QDlM7SHn3BM130_provenance.
- NP724399.RAxEScofSCjh29k3v5SvyFj5C3VViNvGP8QDlM7SHn3BM130_assertion wasGeneratedBy ECO_0000203 NP724399.RAxEScofSCjh29k3v5SvyFj5C3VViNvGP8QDlM7SHn3BM130_provenance.
- befree-20150227 importedOn "2015-02-27" NP724399.RAxEScofSCjh29k3v5SvyFj5C3VViNvGP8QDlM7SHn3BM130_provenance.