Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP547050.RAeq6yGjh3jVxiSMeILCBg32_uRS6eGD4PsBcUJvw4fwo130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP547050.RAeq6yGjh3jVxiSMeILCBg32_uRS6eGD4PsBcUJvw4fwo130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP547050.RAeq6yGjh3jVxiSMeILCBg32_uRS6eGD4PsBcUJvw4fwo130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP547050.RAeq6yGjh3jVxiSMeILCBg32_uRS6eGD4PsBcUJvw4fwo130_provenance.
- NP547050.RAeq6yGjh3jVxiSMeILCBg32_uRS6eGD4PsBcUJvw4fwo130_assertion description "[This includes the discovery that the pathological changes in atypical FTLD with ubiquitinated inclusions, neuronal intermediate filament inclusion disease, and basophilic inclusion body disease are immunoreactive for the fused in sarcoma (FUS) protein, resulting in the creation of a new molecular subgroup (FTLD-FUS), and studies clarifying the functional consequences of pathogenic CHMP2B mutations.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP547050.RAeq6yGjh3jVxiSMeILCBg32_uRS6eGD4PsBcUJvw4fwo130_provenance.
- NP547050.RAeq6yGjh3jVxiSMeILCBg32_uRS6eGD4PsBcUJvw4fwo130_assertion evidence source_evidence_literature NP547050.RAeq6yGjh3jVxiSMeILCBg32_uRS6eGD4PsBcUJvw4fwo130_provenance.
- NP547050.RAeq6yGjh3jVxiSMeILCBg32_uRS6eGD4PsBcUJvw4fwo130_assertion SIO_000772 21603977 NP547050.RAeq6yGjh3jVxiSMeILCBg32_uRS6eGD4PsBcUJvw4fwo130_provenance.
- NP547050.RAeq6yGjh3jVxiSMeILCBg32_uRS6eGD4PsBcUJvw4fwo130_assertion wasDerivedFrom befree-20140225 NP547050.RAeq6yGjh3jVxiSMeILCBg32_uRS6eGD4PsBcUJvw4fwo130_provenance.
- NP547050.RAeq6yGjh3jVxiSMeILCBg32_uRS6eGD4PsBcUJvw4fwo130_assertion wasGeneratedBy ECO_0000203 NP547050.RAeq6yGjh3jVxiSMeILCBg32_uRS6eGD4PsBcUJvw4fwo130_provenance.
- befree-20140225 importedOn "2014-02-25" NP547050.RAeq6yGjh3jVxiSMeILCBg32_uRS6eGD4PsBcUJvw4fwo130_provenance.