Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP276880.RAVR_PMoyqO3VdOs6YmvOXb34p9G0p3ewg4dkCEkUZGz4130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP276880.RAVR_PMoyqO3VdOs6YmvOXb34p9G0p3ewg4dkCEkUZGz4130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP276880.RAVR_PMoyqO3VdOs6YmvOXb34p9G0p3ewg4dkCEkUZGz4130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP276880.RAVR_PMoyqO3VdOs6YmvOXb34p9G0p3ewg4dkCEkUZGz4130_provenance.
- NP276880.RAVR_PMoyqO3VdOs6YmvOXb34p9G0p3ewg4dkCEkUZGz4130_assertion description "[In contrast, mutations in two members of the TFIIH complex, the XPB and XPD genes are generally very severe with both skin and CNS disorders.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP276880.RAVR_PMoyqO3VdOs6YmvOXb34p9G0p3ewg4dkCEkUZGz4130_provenance.
- NP276880.RAVR_PMoyqO3VdOs6YmvOXb34p9G0p3ewg4dkCEkUZGz4130_assertion evidence source_evidence_literature NP276880.RAVR_PMoyqO3VdOs6YmvOXb34p9G0p3ewg4dkCEkUZGz4130_provenance.
- NP276880.RAVR_PMoyqO3VdOs6YmvOXb34p9G0p3ewg4dkCEkUZGz4130_assertion SIO_000772 10699759 NP276880.RAVR_PMoyqO3VdOs6YmvOXb34p9G0p3ewg4dkCEkUZGz4130_provenance.
- NP276880.RAVR_PMoyqO3VdOs6YmvOXb34p9G0p3ewg4dkCEkUZGz4130_assertion wasDerivedFrom befree-2016 NP276880.RAVR_PMoyqO3VdOs6YmvOXb34p9G0p3ewg4dkCEkUZGz4130_provenance.
- NP276880.RAVR_PMoyqO3VdOs6YmvOXb34p9G0p3ewg4dkCEkUZGz4130_assertion wasGeneratedBy ECO_0000203 NP276880.RAVR_PMoyqO3VdOs6YmvOXb34p9G0p3ewg4dkCEkUZGz4130_provenance.
- befree-2016 importedOn "2016-02-19" NP276880.RAVR_PMoyqO3VdOs6YmvOXb34p9G0p3ewg4dkCEkUZGz4130_provenance.