Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP646099.RApA7njBXKG0-F1tgPpzEPVMdUb322rP4YlZvTJ5fhkVQ130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP646099.RApA7njBXKG0-F1tgPpzEPVMdUb322rP4YlZvTJ5fhkVQ130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP646099.RApA7njBXKG0-F1tgPpzEPVMdUb322rP4YlZvTJ5fhkVQ130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP646099.RApA7njBXKG0-F1tgPpzEPVMdUb322rP4YlZvTJ5fhkVQ130_provenance.
- NP646099.RApA7njBXKG0-F1tgPpzEPVMdUb322rP4YlZvTJ5fhkVQ130_assertion description "[A number of families have been reported with autosomal dominant FTD-ALS linked to chromosome 9p and these also have TDP-43-positive frontotemporal lobar degeneration with ubiquitinated inclusions pathology.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP646099.RApA7njBXKG0-F1tgPpzEPVMdUb322rP4YlZvTJ5fhkVQ130_provenance.
- NP646099.RApA7njBXKG0-F1tgPpzEPVMdUb322rP4YlZvTJ5fhkVQ130_assertion evidence source_evidence_literature NP646099.RApA7njBXKG0-F1tgPpzEPVMdUb322rP4YlZvTJ5fhkVQ130_provenance.
- NP646099.RApA7njBXKG0-F1tgPpzEPVMdUb322rP4YlZvTJ5fhkVQ130_assertion SIO_000772 18090423 NP646099.RApA7njBXKG0-F1tgPpzEPVMdUb322rP4YlZvTJ5fhkVQ130_provenance.
- NP646099.RApA7njBXKG0-F1tgPpzEPVMdUb322rP4YlZvTJ5fhkVQ130_assertion wasDerivedFrom befree-2016 NP646099.RApA7njBXKG0-F1tgPpzEPVMdUb322rP4YlZvTJ5fhkVQ130_provenance.
- NP646099.RApA7njBXKG0-F1tgPpzEPVMdUb322rP4YlZvTJ5fhkVQ130_assertion wasGeneratedBy ECO_0000203 NP646099.RApA7njBXKG0-F1tgPpzEPVMdUb322rP4YlZvTJ5fhkVQ130_provenance.
- befree-2016 importedOn "2016-02-19" NP646099.RApA7njBXKG0-F1tgPpzEPVMdUb322rP4YlZvTJ5fhkVQ130_provenance.