Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP567140.RAp8HNc-zdLCHvAoJdyrClDL8d3wO9VnJrOVuN4pe5vck130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP567140.RAp8HNc-zdLCHvAoJdyrClDL8d3wO9VnJrOVuN4pe5vck130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP567140.RAp8HNc-zdLCHvAoJdyrClDL8d3wO9VnJrOVuN4pe5vck130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP567140.RAp8HNc-zdLCHvAoJdyrClDL8d3wO9VnJrOVuN4pe5vck130_provenance.
- NP567140.RAp8HNc-zdLCHvAoJdyrClDL8d3wO9VnJrOVuN4pe5vck130_assertion description "[Phenotypic heterogeneity in the XPB DNA helicase gene (ERCC3): xeroderma pigmentosum without and with Cockayne syndrome.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP567140.RAp8HNc-zdLCHvAoJdyrClDL8d3wO9VnJrOVuN4pe5vck130_provenance.
- NP567140.RAp8HNc-zdLCHvAoJdyrClDL8d3wO9VnJrOVuN4pe5vck130_assertion evidence source_evidence_literature NP567140.RAp8HNc-zdLCHvAoJdyrClDL8d3wO9VnJrOVuN4pe5vck130_provenance.
- NP567140.RAp8HNc-zdLCHvAoJdyrClDL8d3wO9VnJrOVuN4pe5vck130_assertion SIO_000772 16947863 NP567140.RAp8HNc-zdLCHvAoJdyrClDL8d3wO9VnJrOVuN4pe5vck130_provenance.
- NP567140.RAp8HNc-zdLCHvAoJdyrClDL8d3wO9VnJrOVuN4pe5vck130_assertion wasDerivedFrom befree-2016 NP567140.RAp8HNc-zdLCHvAoJdyrClDL8d3wO9VnJrOVuN4pe5vck130_provenance.
- NP567140.RAp8HNc-zdLCHvAoJdyrClDL8d3wO9VnJrOVuN4pe5vck130_assertion wasGeneratedBy ECO_0000203 NP567140.RAp8HNc-zdLCHvAoJdyrClDL8d3wO9VnJrOVuN4pe5vck130_provenance.
- befree-2016 importedOn "2016-02-19" NP567140.RAp8HNc-zdLCHvAoJdyrClDL8d3wO9VnJrOVuN4pe5vck130_provenance.