Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP896088.RALWf-BdYm39dBwE5u6GmOTicQKh3nzjrPItPCGx8rgns130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP896088.RALWf-BdYm39dBwE5u6GmOTicQKh3nzjrPItPCGx8rgns130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP896088.RALWf-BdYm39dBwE5u6GmOTicQKh3nzjrPItPCGx8rgns130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP896088.RALWf-BdYm39dBwE5u6GmOTicQKh3nzjrPItPCGx8rgns130_provenance.
- NP896088.RALWf-BdYm39dBwE5u6GmOTicQKh3nzjrPItPCGx8rgns130_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." NP896088.RALWf-BdYm39dBwE5u6GmOTicQKh3nzjrPItPCGx8rgns130_provenance.
- NP896088.RALWf-BdYm39dBwE5u6GmOTicQKh3nzjrPItPCGx8rgns130_assertion evidence source_evidence_literature NP896088.RALWf-BdYm39dBwE5u6GmOTicQKh3nzjrPItPCGx8rgns130_provenance.
- NP896088.RALWf-BdYm39dBwE5u6GmOTicQKh3nzjrPItPCGx8rgns130_assertion SIO_000772 21603977 NP896088.RALWf-BdYm39dBwE5u6GmOTicQKh3nzjrPItPCGx8rgns130_provenance.
- NP896088.RALWf-BdYm39dBwE5u6GmOTicQKh3nzjrPItPCGx8rgns130_assertion wasDerivedFrom befree-2016 NP896088.RALWf-BdYm39dBwE5u6GmOTicQKh3nzjrPItPCGx8rgns130_provenance.
- NP896088.RALWf-BdYm39dBwE5u6GmOTicQKh3nzjrPItPCGx8rgns130_assertion wasGeneratedBy ECO_0000203 NP896088.RALWf-BdYm39dBwE5u6GmOTicQKh3nzjrPItPCGx8rgns130_provenance.
- befree-2016 importedOn "2016-02-19" NP896088.RALWf-BdYm39dBwE5u6GmOTicQKh3nzjrPItPCGx8rgns130_provenance.