Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP909490.RABl7yamYOrrhVU2TbXnAIKgOpeTuDOvsNkiWL6PvIUDc130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP909490.RABl7yamYOrrhVU2TbXnAIKgOpeTuDOvsNkiWL6PvIUDc130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP909490.RABl7yamYOrrhVU2TbXnAIKgOpeTuDOvsNkiWL6PvIUDc130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP909490.RABl7yamYOrrhVU2TbXnAIKgOpeTuDOvsNkiWL6PvIUDc130_provenance.
- befree-2016 importedOn "2016-02-19" NP909490.RABl7yamYOrrhVU2TbXnAIKgOpeTuDOvsNkiWL6PvIUDc130_provenance.
- NP909490.RABl7yamYOrrhVU2TbXnAIKgOpeTuDOvsNkiWL6PvIUDc130_assertion wasGeneratedBy ECO_0000203 NP909490.RABl7yamYOrrhVU2TbXnAIKgOpeTuDOvsNkiWL6PvIUDc130_provenance.
- NP909490.RABl7yamYOrrhVU2TbXnAIKgOpeTuDOvsNkiWL6PvIUDc130_assertion wasDerivedFrom befree-2016 NP909490.RABl7yamYOrrhVU2TbXnAIKgOpeTuDOvsNkiWL6PvIUDc130_provenance.
- NP909490.RABl7yamYOrrhVU2TbXnAIKgOpeTuDOvsNkiWL6PvIUDc130_assertion SIO_000772 21752791 NP909490.RABl7yamYOrrhVU2TbXnAIKgOpeTuDOvsNkiWL6PvIUDc130_provenance.
- NP909490.RABl7yamYOrrhVU2TbXnAIKgOpeTuDOvsNkiWL6PvIUDc130_assertion evidence source_evidence_literature NP909490.RABl7yamYOrrhVU2TbXnAIKgOpeTuDOvsNkiWL6PvIUDc130_provenance.
- NP909490.RABl7yamYOrrhVU2TbXnAIKgOpeTuDOvsNkiWL6PvIUDc130_assertion description "[Recently, mutations in the fused in sarcoma gene have been shown to cause familial amyotrophic lateral sclerosis and fused in sarcoma-positive neuronal inclusions have subsequently been demonstrated in neuronal intermediate filament inclusion disease and atypical frontotemporal lobar degeneration with ubiquitinated inclusions.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP909490.RABl7yamYOrrhVU2TbXnAIKgOpeTuDOvsNkiWL6PvIUDc130_provenance.