Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP418963.RAna8nbPkguAmj8zQMXkmeVuUUSjyNvyh_duVvZ1KtnmQ130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP418963.RAna8nbPkguAmj8zQMXkmeVuUUSjyNvyh_duVvZ1KtnmQ130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP418963.RAna8nbPkguAmj8zQMXkmeVuUUSjyNvyh_duVvZ1KtnmQ130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP418963.RAna8nbPkguAmj8zQMXkmeVuUUSjyNvyh_duVvZ1KtnmQ130_provenance.
- NP418963.RAna8nbPkguAmj8zQMXkmeVuUUSjyNvyh_duVvZ1KtnmQ130_assertion description "[Moreover, when XPD mutations prevent interaction with the p44 subunit of TFIIH, transactivation directed by certain nuclear receptors is inhibited, regardless of TTD versus XP phenotype, thus explaining the overlapping symptoms.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP418963.RAna8nbPkguAmj8zQMXkmeVuUUSjyNvyh_duVvZ1KtnmQ130_provenance.
- NP418963.RAna8nbPkguAmj8zQMXkmeVuUUSjyNvyh_duVvZ1KtnmQ130_assertion evidence source_evidence_literature NP418963.RAna8nbPkguAmj8zQMXkmeVuUUSjyNvyh_duVvZ1KtnmQ130_provenance.
- NP418963.RAna8nbPkguAmj8zQMXkmeVuUUSjyNvyh_duVvZ1KtnmQ130_assertion SIO_000772 12820975 NP418963.RAna8nbPkguAmj8zQMXkmeVuUUSjyNvyh_duVvZ1KtnmQ130_provenance.
- NP418963.RAna8nbPkguAmj8zQMXkmeVuUUSjyNvyh_duVvZ1KtnmQ130_assertion wasDerivedFrom befree-20140225 NP418963.RAna8nbPkguAmj8zQMXkmeVuUUSjyNvyh_duVvZ1KtnmQ130_provenance.
- NP418963.RAna8nbPkguAmj8zQMXkmeVuUUSjyNvyh_duVvZ1KtnmQ130_assertion wasGeneratedBy ECO_0000203 NP418963.RAna8nbPkguAmj8zQMXkmeVuUUSjyNvyh_duVvZ1KtnmQ130_provenance.
- befree-20140225 importedOn "2014-02-25" NP418963.RAna8nbPkguAmj8zQMXkmeVuUUSjyNvyh_duVvZ1KtnmQ130_provenance.