Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP179619.RAX_e4HYdbVT-KwVXIEfGmdMrOlq1j7XkQKsQ1ucIsLag130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP179619.RAX_e4HYdbVT-KwVXIEfGmdMrOlq1j7XkQKsQ1ucIsLag130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP179619.RAX_e4HYdbVT-KwVXIEfGmdMrOlq1j7XkQKsQ1ucIsLag130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP179619.RAX_e4HYdbVT-KwVXIEfGmdMrOlq1j7XkQKsQ1ucIsLag130_provenance.
- NP179619.RAX_e4HYdbVT-KwVXIEfGmdMrOlq1j7XkQKsQ1ucIsLag130_assertion description "[Clinical comparison of SOD1, TARDBP, FUS and other familial ALS patients (with no mutation in the screened genes) revealed differences in site of onset (predominantly lower limbs for SOD1 and upper limbs for TARDBP mutations), age of onset (younger with FUS mutations), and in lifespan (shorter for FUS carriers).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP179619.RAX_e4HYdbVT-KwVXIEfGmdMrOlq1j7XkQKsQ1ucIsLag130_provenance.
- NP179619.RAX_e4HYdbVT-KwVXIEfGmdMrOlq1j7XkQKsQ1ucIsLag130_assertion evidence source_evidence_literature NP179619.RAX_e4HYdbVT-KwVXIEfGmdMrOlq1j7XkQKsQ1ucIsLag130_provenance.
- NP179619.RAX_e4HYdbVT-KwVXIEfGmdMrOlq1j7XkQKsQ1ucIsLag130_assertion SIO_000772 20577002 NP179619.RAX_e4HYdbVT-KwVXIEfGmdMrOlq1j7XkQKsQ1ucIsLag130_provenance.
- NP179619.RAX_e4HYdbVT-KwVXIEfGmdMrOlq1j7XkQKsQ1ucIsLag130_assertion wasDerivedFrom gad-20150221 NP179619.RAX_e4HYdbVT-KwVXIEfGmdMrOlq1j7XkQKsQ1ucIsLag130_provenance.
- NP179619.RAX_e4HYdbVT-KwVXIEfGmdMrOlq1j7XkQKsQ1ucIsLag130_assertion wasGeneratedBy ECO_0000203 NP179619.RAX_e4HYdbVT-KwVXIEfGmdMrOlq1j7XkQKsQ1ucIsLag130_provenance.
- gad-20150221 importedOn "2015-02-21" NP179619.RAX_e4HYdbVT-KwVXIEfGmdMrOlq1j7XkQKsQ1ucIsLag130_provenance.