Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP381814.RAzO15WO0aybS61BxqCOr6TBgDrcQOBywPZIPvW-ltVLc130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP381814.RAzO15WO0aybS61BxqCOr6TBgDrcQOBywPZIPvW-ltVLc130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP381814.RAzO15WO0aybS61BxqCOr6TBgDrcQOBywPZIPvW-ltVLc130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP381814.RAzO15WO0aybS61BxqCOr6TBgDrcQOBywPZIPvW-ltVLc130_provenance.
- NP381814.RAzO15WO0aybS61BxqCOr6TBgDrcQOBywPZIPvW-ltVLc130_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." NP381814.RAzO15WO0aybS61BxqCOr6TBgDrcQOBywPZIPvW-ltVLc130_provenance.
- NP381814.RAzO15WO0aybS61BxqCOr6TBgDrcQOBywPZIPvW-ltVLc130_assertion evidence source_evidence_literature NP381814.RAzO15WO0aybS61BxqCOr6TBgDrcQOBywPZIPvW-ltVLc130_provenance.
- NP381814.RAzO15WO0aybS61BxqCOr6TBgDrcQOBywPZIPvW-ltVLc130_assertion SIO_000772 16646069 NP381814.RAzO15WO0aybS61BxqCOr6TBgDrcQOBywPZIPvW-ltVLc130_provenance.
- NP381814.RAzO15WO0aybS61BxqCOr6TBgDrcQOBywPZIPvW-ltVLc130_assertion wasDerivedFrom befree-20150227 NP381814.RAzO15WO0aybS61BxqCOr6TBgDrcQOBywPZIPvW-ltVLc130_provenance.
- NP381814.RAzO15WO0aybS61BxqCOr6TBgDrcQOBywPZIPvW-ltVLc130_assertion wasGeneratedBy ECO_0000203 NP381814.RAzO15WO0aybS61BxqCOr6TBgDrcQOBywPZIPvW-ltVLc130_provenance.
- befree-20150227 importedOn "2015-02-27" NP381814.RAzO15WO0aybS61BxqCOr6TBgDrcQOBywPZIPvW-ltVLc130_provenance.