Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP800603.RAdKbVrImyI_unHnXHrLWecgPLbwUNf2UBg1QmiVaeSVQ130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP800603.RAdKbVrImyI_unHnXHrLWecgPLbwUNf2UBg1QmiVaeSVQ130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP800603.RAdKbVrImyI_unHnXHrLWecgPLbwUNf2UBg1QmiVaeSVQ130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP800603.RAdKbVrImyI_unHnXHrLWecgPLbwUNf2UBg1QmiVaeSVQ130_provenance.
- NP800603.RAdKbVrImyI_unHnXHrLWecgPLbwUNf2UBg1QmiVaeSVQ130_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." NP800603.RAdKbVrImyI_unHnXHrLWecgPLbwUNf2UBg1QmiVaeSVQ130_provenance.
- NP800603.RAdKbVrImyI_unHnXHrLWecgPLbwUNf2UBg1QmiVaeSVQ130_assertion evidence source_evidence_literature NP800603.RAdKbVrImyI_unHnXHrLWecgPLbwUNf2UBg1QmiVaeSVQ130_provenance.
- NP800603.RAdKbVrImyI_unHnXHrLWecgPLbwUNf2UBg1QmiVaeSVQ130_assertion SIO_000772 20236864 NP800603.RAdKbVrImyI_unHnXHrLWecgPLbwUNf2UBg1QmiVaeSVQ130_provenance.
- NP800603.RAdKbVrImyI_unHnXHrLWecgPLbwUNf2UBg1QmiVaeSVQ130_assertion wasDerivedFrom befree-2016 NP800603.RAdKbVrImyI_unHnXHrLWecgPLbwUNf2UBg1QmiVaeSVQ130_provenance.
- NP800603.RAdKbVrImyI_unHnXHrLWecgPLbwUNf2UBg1QmiVaeSVQ130_assertion wasGeneratedBy ECO_0000203 NP800603.RAdKbVrImyI_unHnXHrLWecgPLbwUNf2UBg1QmiVaeSVQ130_provenance.
- befree-2016 importedOn "2016-02-19" NP800603.RAdKbVrImyI_unHnXHrLWecgPLbwUNf2UBg1QmiVaeSVQ130_provenance.