Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP382715.RAzU2O32zsP-c14hpH3l9VuUYoiGM8MrrQ9xmFEMipW54130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP382715.RAzU2O32zsP-c14hpH3l9VuUYoiGM8MrrQ9xmFEMipW54130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP382715.RAzU2O32zsP-c14hpH3l9VuUYoiGM8MrrQ9xmFEMipW54130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP382715.RAzU2O32zsP-c14hpH3l9VuUYoiGM8MrrQ9xmFEMipW54130_provenance.
- NP382715.RAzU2O32zsP-c14hpH3l9VuUYoiGM8MrrQ9xmFEMipW54130_assertion description "[NER involves more than 20 proteins whose inactivation leads to xeroderma pigmentosum (XP) or cockayne syndrome (CS), among which XPD, a helicase allowing DNA strand excision by the endonuclease XPG.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP382715.RAzU2O32zsP-c14hpH3l9VuUYoiGM8MrrQ9xmFEMipW54130_provenance.
- NP382715.RAzU2O32zsP-c14hpH3l9VuUYoiGM8MrrQ9xmFEMipW54130_assertion evidence source_evidence_literature NP382715.RAzU2O32zsP-c14hpH3l9VuUYoiGM8MrrQ9xmFEMipW54130_provenance.
- NP382715.RAzU2O32zsP-c14hpH3l9VuUYoiGM8MrrQ9xmFEMipW54130_assertion SIO_000772 16646069 NP382715.RAzU2O32zsP-c14hpH3l9VuUYoiGM8MrrQ9xmFEMipW54130_provenance.
- NP382715.RAzU2O32zsP-c14hpH3l9VuUYoiGM8MrrQ9xmFEMipW54130_assertion wasDerivedFrom befree-20150227 NP382715.RAzU2O32zsP-c14hpH3l9VuUYoiGM8MrrQ9xmFEMipW54130_provenance.
- NP382715.RAzU2O32zsP-c14hpH3l9VuUYoiGM8MrrQ9xmFEMipW54130_assertion wasGeneratedBy ECO_0000203 NP382715.RAzU2O32zsP-c14hpH3l9VuUYoiGM8MrrQ9xmFEMipW54130_provenance.
- befree-20150227 importedOn "2015-02-27" NP382715.RAzU2O32zsP-c14hpH3l9VuUYoiGM8MrrQ9xmFEMipW54130_provenance.