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- source_evidence_literature type ECO_0000212 NP1244135.RAfb8YjfrtEdDC_Sa6_-NK9eYRDzz9xYoeCT8-af8E9gY130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP1244135.RAfb8YjfrtEdDC_Sa6_-NK9eYRDzz9xYoeCT8-af8E9gY130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP1244135.RAfb8YjfrtEdDC_Sa6_-NK9eYRDzz9xYoeCT8-af8E9gY130_provenance.
- NP1244135.RAfb8YjfrtEdDC_Sa6_-NK9eYRDzz9xYoeCT8-af8E9gY130_assertion description "[The GGGGCC hexanucleotide expansion in the C9ORF72 gene is the most common cause of familial amyotrophic lateral sclerosis (ALS) and frontotemporal dementia (FTD) in Caucasian populations.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1244135.RAfb8YjfrtEdDC_Sa6_-NK9eYRDzz9xYoeCT8-af8E9gY130_provenance.
- NP1244135.RAfb8YjfrtEdDC_Sa6_-NK9eYRDzz9xYoeCT8-af8E9gY130_assertion evidence source_evidence_literature NP1244135.RAfb8YjfrtEdDC_Sa6_-NK9eYRDzz9xYoeCT8-af8E9gY130_provenance.
- NP1244135.RAfb8YjfrtEdDC_Sa6_-NK9eYRDzz9xYoeCT8-af8E9gY130_assertion SIO_000772 25467142 NP1244135.RAfb8YjfrtEdDC_Sa6_-NK9eYRDzz9xYoeCT8-af8E9gY130_provenance.
- NP1244135.RAfb8YjfrtEdDC_Sa6_-NK9eYRDzz9xYoeCT8-af8E9gY130_assertion wasDerivedFrom befree-2016 NP1244135.RAfb8YjfrtEdDC_Sa6_-NK9eYRDzz9xYoeCT8-af8E9gY130_provenance.
- NP1244135.RAfb8YjfrtEdDC_Sa6_-NK9eYRDzz9xYoeCT8-af8E9gY130_assertion wasGeneratedBy ECO_0000203 NP1244135.RAfb8YjfrtEdDC_Sa6_-NK9eYRDzz9xYoeCT8-af8E9gY130_provenance.
- befree-2016 importedOn "2016-02-19" NP1244135.RAfb8YjfrtEdDC_Sa6_-NK9eYRDzz9xYoeCT8-af8E9gY130_provenance.