Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP382416.RAS6JkBffEM4ZY1CQTGY6vnaaaxH2xE3fl7M6FacEILQ8130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP382416.RAS6JkBffEM4ZY1CQTGY6vnaaaxH2xE3fl7M6FacEILQ8130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP382416.RAS6JkBffEM4ZY1CQTGY6vnaaaxH2xE3fl7M6FacEILQ8130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP382416.RAS6JkBffEM4ZY1CQTGY6vnaaaxH2xE3fl7M6FacEILQ8130_provenance.
- NP382416.RAS6JkBffEM4ZY1CQTGY6vnaaaxH2xE3fl7M6FacEILQ8130_assertion description "[For the rare combined xeroderma pigmentosum (XP) and CS phenotype, all identified mutations are in three of the XP-associated genes, ERCC3 (XPB), ERCC2 (XPD), and ERCC5 (XPG).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP382416.RAS6JkBffEM4ZY1CQTGY6vnaaaxH2xE3fl7M6FacEILQ8130_provenance.
- NP382416.RAS6JkBffEM4ZY1CQTGY6vnaaaxH2xE3fl7M6FacEILQ8130_assertion evidence source_evidence_literature NP382416.RAS6JkBffEM4ZY1CQTGY6vnaaaxH2xE3fl7M6FacEILQ8130_provenance.
- NP382416.RAS6JkBffEM4ZY1CQTGY6vnaaaxH2xE3fl7M6FacEILQ8130_assertion SIO_000772 23623389 NP382416.RAS6JkBffEM4ZY1CQTGY6vnaaaxH2xE3fl7M6FacEILQ8130_provenance.
- NP382416.RAS6JkBffEM4ZY1CQTGY6vnaaaxH2xE3fl7M6FacEILQ8130_assertion wasDerivedFrom befree-20150227 NP382416.RAS6JkBffEM4ZY1CQTGY6vnaaaxH2xE3fl7M6FacEILQ8130_provenance.
- NP382416.RAS6JkBffEM4ZY1CQTGY6vnaaaxH2xE3fl7M6FacEILQ8130_assertion wasGeneratedBy ECO_0000203 NP382416.RAS6JkBffEM4ZY1CQTGY6vnaaaxH2xE3fl7M6FacEILQ8130_provenance.
- befree-20150227 importedOn "2015-02-27" NP382416.RAS6JkBffEM4ZY1CQTGY6vnaaaxH2xE3fl7M6FacEILQ8130_provenance.