Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP269783.RAhaH-mariVz-R7kTWabp-OUJbCERAzl3j7FLF5rRLbWo130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP269783.RAhaH-mariVz-R7kTWabp-OUJbCERAzl3j7FLF5rRLbWo130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP269783.RAhaH-mariVz-R7kTWabp-OUJbCERAzl3j7FLF5rRLbWo130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP269783.RAhaH-mariVz-R7kTWabp-OUJbCERAzl3j7FLF5rRLbWo130_provenance.
- befree-2016 importedOn "2016-02-19" NP269783.RAhaH-mariVz-R7kTWabp-OUJbCERAzl3j7FLF5rRLbWo130_provenance.
- NP269783.RAhaH-mariVz-R7kTWabp-OUJbCERAzl3j7FLF5rRLbWo130_assertion wasGeneratedBy ECO_0000203 NP269783.RAhaH-mariVz-R7kTWabp-OUJbCERAzl3j7FLF5rRLbWo130_provenance.
- NP269783.RAhaH-mariVz-R7kTWabp-OUJbCERAzl3j7FLF5rRLbWo130_assertion wasDerivedFrom befree-2016 NP269783.RAhaH-mariVz-R7kTWabp-OUJbCERAzl3j7FLF5rRLbWo130_provenance.
- NP269783.RAhaH-mariVz-R7kTWabp-OUJbCERAzl3j7FLF5rRLbWo130_assertion SIO_000772 10597140 NP269783.RAhaH-mariVz-R7kTWabp-OUJbCERAzl3j7FLF5rRLbWo130_provenance.
- NP269783.RAhaH-mariVz-R7kTWabp-OUJbCERAzl3j7FLF5rRLbWo130_assertion evidence source_evidence_literature NP269783.RAhaH-mariVz-R7kTWabp-OUJbCERAzl3j7FLF5rRLbWo130_provenance.
- NP269783.RAhaH-mariVz-R7kTWabp-OUJbCERAzl3j7FLF5rRLbWo130_assertion description "[Epidermolytic hyperkeratosis (EHK) is a genodermatosis caused by mutations in either the keratin 1 (K1) or keratin 10 (K10) genes, and characterized by erythroderma and blistering at birth, with development of a ribbed, ichthyotic hyperkeratosis and palmoplantar keratoderma.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP269783.RAhaH-mariVz-R7kTWabp-OUJbCERAzl3j7FLF5rRLbWo130_provenance.