Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP610178.RA1Cy_tv_8JR3ppA0RDYcdxV3vriYsP0OAftqw-NDX3Dg130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP610178.RA1Cy_tv_8JR3ppA0RDYcdxV3vriYsP0OAftqw-NDX3Dg130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP610178.RA1Cy_tv_8JR3ppA0RDYcdxV3vriYsP0OAftqw-NDX3Dg130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP610178.RA1Cy_tv_8JR3ppA0RDYcdxV3vriYsP0OAftqw-NDX3Dg130_provenance.
- NP610178.RA1Cy_tv_8JR3ppA0RDYcdxV3vriYsP0OAftqw-NDX3Dg130_assertion description "[Moreover, mutations in any of these three TFIIH subunits also disturb the overall architecture of the TFIIH complex and its ability to transactivate certain nuclear receptor-responsive genes, explaining in part, some of the TTD phenotypes.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP610178.RA1Cy_tv_8JR3ppA0RDYcdxV3vriYsP0OAftqw-NDX3Dg130_provenance.
- NP610178.RA1Cy_tv_8JR3ppA0RDYcdxV3vriYsP0OAftqw-NDX3Dg130_assertion evidence source_evidence_literature NP610178.RA1Cy_tv_8JR3ppA0RDYcdxV3vriYsP0OAftqw-NDX3Dg130_provenance.
- NP610178.RA1Cy_tv_8JR3ppA0RDYcdxV3vriYsP0OAftqw-NDX3Dg130_assertion SIO_000772 19808800 NP610178.RA1Cy_tv_8JR3ppA0RDYcdxV3vriYsP0OAftqw-NDX3Dg130_provenance.
- NP610178.RA1Cy_tv_8JR3ppA0RDYcdxV3vriYsP0OAftqw-NDX3Dg130_assertion wasDerivedFrom befree-20140225 NP610178.RA1Cy_tv_8JR3ppA0RDYcdxV3vriYsP0OAftqw-NDX3Dg130_provenance.
- NP610178.RA1Cy_tv_8JR3ppA0RDYcdxV3vriYsP0OAftqw-NDX3Dg130_assertion wasGeneratedBy ECO_0000203 NP610178.RA1Cy_tv_8JR3ppA0RDYcdxV3vriYsP0OAftqw-NDX3Dg130_provenance.
- befree-20140225 importedOn "2014-02-25" NP610178.RA1Cy_tv_8JR3ppA0RDYcdxV3vriYsP0OAftqw-NDX3Dg130_provenance.