Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP951791.RAhpaAE_MRo6K8cSkprlPiClRIQgMgNfju9vMhFdXOVsQ130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP951791.RAhpaAE_MRo6K8cSkprlPiClRIQgMgNfju9vMhFdXOVsQ130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP951791.RAhpaAE_MRo6K8cSkprlPiClRIQgMgNfju9vMhFdXOVsQ130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP951791.RAhpaAE_MRo6K8cSkprlPiClRIQgMgNfju9vMhFdXOVsQ130_provenance.
- NP951791.RAhpaAE_MRo6K8cSkprlPiClRIQgMgNfju9vMhFdXOVsQ130_assertion description "[Finally, mutations in UNC93B1 and TLR3 are associated with childhood herpes simplex encephalitis, which strikes only once in most patients, with almost no recorded cases of more than two bouts of this disease.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP951791.RAhpaAE_MRo6K8cSkprlPiClRIQgMgNfju9vMhFdXOVsQ130_provenance.
- NP951791.RAhpaAE_MRo6K8cSkprlPiClRIQgMgNfju9vMhFdXOVsQ130_assertion evidence source_evidence_literature NP951791.RAhpaAE_MRo6K8cSkprlPiClRIQgMgNfju9vMhFdXOVsQ130_provenance.
- NP951791.RAhpaAE_MRo6K8cSkprlPiClRIQgMgNfju9vMhFdXOVsQ130_assertion SIO_000772 20236864 NP951791.RAhpaAE_MRo6K8cSkprlPiClRIQgMgNfju9vMhFdXOVsQ130_provenance.
- NP951791.RAhpaAE_MRo6K8cSkprlPiClRIQgMgNfju9vMhFdXOVsQ130_assertion wasDerivedFrom befree-20150227 NP951791.RAhpaAE_MRo6K8cSkprlPiClRIQgMgNfju9vMhFdXOVsQ130_provenance.
- NP951791.RAhpaAE_MRo6K8cSkprlPiClRIQgMgNfju9vMhFdXOVsQ130_assertion wasGeneratedBy ECO_0000203 NP951791.RAhpaAE_MRo6K8cSkprlPiClRIQgMgNfju9vMhFdXOVsQ130_provenance.
- befree-20150227 importedOn "2015-02-27" NP951791.RAhpaAE_MRo6K8cSkprlPiClRIQgMgNfju9vMhFdXOVsQ130_provenance.