Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP281616.RAeXRRTqUkFIcZhXW1eT1Ox9AgW7c5nwTfjJdypLxcbUw130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP281616.RAeXRRTqUkFIcZhXW1eT1Ox9AgW7c5nwTfjJdypLxcbUw130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP281616.RAeXRRTqUkFIcZhXW1eT1Ox9AgW7c5nwTfjJdypLxcbUw130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP281616.RAeXRRTqUkFIcZhXW1eT1Ox9AgW7c5nwTfjJdypLxcbUw130_provenance.
- NP281616.RAeXRRTqUkFIcZhXW1eT1Ox9AgW7c5nwTfjJdypLxcbUw130_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." NP281616.RAeXRRTqUkFIcZhXW1eT1Ox9AgW7c5nwTfjJdypLxcbUw130_provenance.
- NP281616.RAeXRRTqUkFIcZhXW1eT1Ox9AgW7c5nwTfjJdypLxcbUw130_assertion evidence source_evidence_literature NP281616.RAeXRRTqUkFIcZhXW1eT1Ox9AgW7c5nwTfjJdypLxcbUw130_provenance.
- NP281616.RAeXRRTqUkFIcZhXW1eT1Ox9AgW7c5nwTfjJdypLxcbUw130_assertion SIO_000772 12820975 NP281616.RAeXRRTqUkFIcZhXW1eT1Ox9AgW7c5nwTfjJdypLxcbUw130_provenance.
- NP281616.RAeXRRTqUkFIcZhXW1eT1Ox9AgW7c5nwTfjJdypLxcbUw130_assertion wasDerivedFrom befree-20140225 NP281616.RAeXRRTqUkFIcZhXW1eT1Ox9AgW7c5nwTfjJdypLxcbUw130_provenance.
- NP281616.RAeXRRTqUkFIcZhXW1eT1Ox9AgW7c5nwTfjJdypLxcbUw130_assertion wasGeneratedBy ECO_0000203 NP281616.RAeXRRTqUkFIcZhXW1eT1Ox9AgW7c5nwTfjJdypLxcbUw130_provenance.
- befree-20140225 importedOn "2014-02-25" NP281616.RAeXRRTqUkFIcZhXW1eT1Ox9AgW7c5nwTfjJdypLxcbUw130_provenance.