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- source_evidence_literature type ECO_0000212 NP947835.RAtlzZmq8-5-NDlJzPiGJxY-OYbnpOy7avIObFHKG9rys130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP947835.RAtlzZmq8-5-NDlJzPiGJxY-OYbnpOy7avIObFHKG9rys130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP947835.RAtlzZmq8-5-NDlJzPiGJxY-OYbnpOy7avIObFHKG9rys130_provenance.
- NP947835.RAtlzZmq8-5-NDlJzPiGJxY-OYbnpOy7avIObFHKG9rys130_assertion description "[MND/ALS-associated SOD1, FUS and TARDBP gene mutations were excluded; however, further investigations revealed that all four of the cases did show a repeat expansion of C9orf72, the recently reported cause of chromosome 9-linked MND/ALS and FTLD.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP947835.RAtlzZmq8-5-NDlJzPiGJxY-OYbnpOy7avIObFHKG9rys130_provenance.
- NP947835.RAtlzZmq8-5-NDlJzPiGJxY-OYbnpOy7avIObFHKG9rys130_assertion evidence source_evidence_literature NP947835.RAtlzZmq8-5-NDlJzPiGJxY-OYbnpOy7avIObFHKG9rys130_provenance.
- NP947835.RAtlzZmq8-5-NDlJzPiGJxY-OYbnpOy7avIObFHKG9rys130_assertion SIO_000772 22181065 NP947835.RAtlzZmq8-5-NDlJzPiGJxY-OYbnpOy7avIObFHKG9rys130_provenance.
- NP947835.RAtlzZmq8-5-NDlJzPiGJxY-OYbnpOy7avIObFHKG9rys130_assertion wasDerivedFrom befree-2016 NP947835.RAtlzZmq8-5-NDlJzPiGJxY-OYbnpOy7avIObFHKG9rys130_provenance.
- NP947835.RAtlzZmq8-5-NDlJzPiGJxY-OYbnpOy7avIObFHKG9rys130_assertion wasGeneratedBy ECO_0000203 NP947835.RAtlzZmq8-5-NDlJzPiGJxY-OYbnpOy7avIObFHKG9rys130_provenance.
- befree-2016 importedOn "2016-02-19" NP947835.RAtlzZmq8-5-NDlJzPiGJxY-OYbnpOy7avIObFHKG9rys130_provenance.