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- source_evidence_literature type ECO_0000212 NP1216018.RAwJANoWqR3KUwVMfHzOU-uGehVisiIPof0Mt6uoGgWC0130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP1216018.RAwJANoWqR3KUwVMfHzOU-uGehVisiIPof0Mt6uoGgWC0130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP1216018.RAwJANoWqR3KUwVMfHzOU-uGehVisiIPof0Mt6uoGgWC0130_provenance.
- NP1216018.RAwJANoWqR3KUwVMfHzOU-uGehVisiIPof0Mt6uoGgWC0130_assertion description "[An expanded hexanucleotide repeat in the C9orf72 gene is the most common genetic cause of amyotrophic lateral sclerosis and frontotemporal dementia (C9ALS/FTD).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1216018.RAwJANoWqR3KUwVMfHzOU-uGehVisiIPof0Mt6uoGgWC0130_provenance.
- NP1216018.RAwJANoWqR3KUwVMfHzOU-uGehVisiIPof0Mt6uoGgWC0130_assertion evidence source_evidence_literature NP1216018.RAwJANoWqR3KUwVMfHzOU-uGehVisiIPof0Mt6uoGgWC0130_provenance.
- NP1216018.RAwJANoWqR3KUwVMfHzOU-uGehVisiIPof0Mt6uoGgWC0130_assertion SIO_000772 25179228 NP1216018.RAwJANoWqR3KUwVMfHzOU-uGehVisiIPof0Mt6uoGgWC0130_provenance.
- NP1216018.RAwJANoWqR3KUwVMfHzOU-uGehVisiIPof0Mt6uoGgWC0130_assertion wasDerivedFrom befree-2016 NP1216018.RAwJANoWqR3KUwVMfHzOU-uGehVisiIPof0Mt6uoGgWC0130_provenance.
- NP1216018.RAwJANoWqR3KUwVMfHzOU-uGehVisiIPof0Mt6uoGgWC0130_assertion wasGeneratedBy ECO_0000203 NP1216018.RAwJANoWqR3KUwVMfHzOU-uGehVisiIPof0Mt6uoGgWC0130_provenance.
- befree-2016 importedOn "2016-02-19" NP1216018.RAwJANoWqR3KUwVMfHzOU-uGehVisiIPof0Mt6uoGgWC0130_provenance.