Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP411118.RA6U6dunIYSLHQZXXpTWdFtwuV17Sp0MkdIB4AssennjI130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP411118.RA6U6dunIYSLHQZXXpTWdFtwuV17Sp0MkdIB4AssennjI130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP411118.RA6U6dunIYSLHQZXXpTWdFtwuV17Sp0MkdIB4AssennjI130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP411118.RA6U6dunIYSLHQZXXpTWdFtwuV17Sp0MkdIB4AssennjI130_provenance.
- NP411118.RA6U6dunIYSLHQZXXpTWdFtwuV17Sp0MkdIB4AssennjI130_assertion description "[Cockayne syndrome (CS) is mainly caused by mutations in the Cockayne syndrome group A or B (CSA or CSB) genes which are required for a sub-pathway of nucleotide excision repair entitled transcription coupled repair.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP411118.RA6U6dunIYSLHQZXXpTWdFtwuV17Sp0MkdIB4AssennjI130_provenance.
- NP411118.RA6U6dunIYSLHQZXXpTWdFtwuV17Sp0MkdIB4AssennjI130_assertion evidence source_evidence_literature NP411118.RA6U6dunIYSLHQZXXpTWdFtwuV17Sp0MkdIB4AssennjI130_provenance.
- NP411118.RA6U6dunIYSLHQZXXpTWdFtwuV17Sp0MkdIB4AssennjI130_assertion SIO_000772 17084038 NP411118.RA6U6dunIYSLHQZXXpTWdFtwuV17Sp0MkdIB4AssennjI130_provenance.
- NP411118.RA6U6dunIYSLHQZXXpTWdFtwuV17Sp0MkdIB4AssennjI130_assertion wasDerivedFrom befree-20140225 NP411118.RA6U6dunIYSLHQZXXpTWdFtwuV17Sp0MkdIB4AssennjI130_provenance.
- NP411118.RA6U6dunIYSLHQZXXpTWdFtwuV17Sp0MkdIB4AssennjI130_assertion wasGeneratedBy ECO_0000203 NP411118.RA6U6dunIYSLHQZXXpTWdFtwuV17Sp0MkdIB4AssennjI130_provenance.
- befree-20140225 importedOn "2014-02-25" NP411118.RA6U6dunIYSLHQZXXpTWdFtwuV17Sp0MkdIB4AssennjI130_provenance.