Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP404127.RA-rfiJxoshs0gbZkXreRkBRLRyhKqlK4ifReNjr02FXI130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP404127.RA-rfiJxoshs0gbZkXreRkBRLRyhKqlK4ifReNjr02FXI130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP404127.RA-rfiJxoshs0gbZkXreRkBRLRyhKqlK4ifReNjr02FXI130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP404127.RA-rfiJxoshs0gbZkXreRkBRLRyhKqlK4ifReNjr02FXI130_provenance.
- NP404127.RA-rfiJxoshs0gbZkXreRkBRLRyhKqlK4ifReNjr02FXI130_assertion description "[Mutations in XPA that are within the DNA binding site produce more severe CNS disorders, than mutations in the C-terminal region of the protein that interacts with the TFIIH complex.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP404127.RA-rfiJxoshs0gbZkXreRkBRLRyhKqlK4ifReNjr02FXI130_provenance.
- NP404127.RA-rfiJxoshs0gbZkXreRkBRLRyhKqlK4ifReNjr02FXI130_assertion evidence source_evidence_literature NP404127.RA-rfiJxoshs0gbZkXreRkBRLRyhKqlK4ifReNjr02FXI130_provenance.
- NP404127.RA-rfiJxoshs0gbZkXreRkBRLRyhKqlK4ifReNjr02FXI130_assertion SIO_000772 10699759 NP404127.RA-rfiJxoshs0gbZkXreRkBRLRyhKqlK4ifReNjr02FXI130_provenance.
- NP404127.RA-rfiJxoshs0gbZkXreRkBRLRyhKqlK4ifReNjr02FXI130_assertion wasDerivedFrom befree-20140225 NP404127.RA-rfiJxoshs0gbZkXreRkBRLRyhKqlK4ifReNjr02FXI130_provenance.
- NP404127.RA-rfiJxoshs0gbZkXreRkBRLRyhKqlK4ifReNjr02FXI130_assertion wasGeneratedBy ECO_0000203 NP404127.RA-rfiJxoshs0gbZkXreRkBRLRyhKqlK4ifReNjr02FXI130_provenance.
- befree-20140225 importedOn "2014-02-25" NP404127.RA-rfiJxoshs0gbZkXreRkBRLRyhKqlK4ifReNjr02FXI130_provenance.