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- source_evidence_literature type ECO_0000212 NP83500.RAIEAf_HM91OJfXG7JUubGHmC9hAU4zQX76nw0kuquOso130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP83500.RAIEAf_HM91OJfXG7JUubGHmC9hAU4zQX76nw0kuquOso130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP83500.RAIEAf_HM91OJfXG7JUubGHmC9hAU4zQX76nw0kuquOso130_provenance.
- NP83500.RAIEAf_HM91OJfXG7JUubGHmC9hAU4zQX76nw0kuquOso130_assertion description "[ To our knowledge, this is the first report of SPG4 mutations in the People's Republic of China. The percentage of involved Chinese families with autosomal dominant hereditary spastic paraplegia with an SPG4 mutation is 18% (4/22), lower than the estimate]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP83500.RAIEAf_HM91OJfXG7JUubGHmC9hAU4zQX76nw0kuquOso130_provenance.
- NP83500.RAIEAf_HM91OJfXG7JUubGHmC9hAU4zQX76nw0kuquOso130_assertion evidence source_evidence_literature NP83500.RAIEAf_HM91OJfXG7JUubGHmC9hAU4zQX76nw0kuquOso130_provenance.
- NP83500.RAIEAf_HM91OJfXG7JUubGHmC9hAU4zQX76nw0kuquOso130_assertion SIO_000772 14732620 NP83500.RAIEAf_HM91OJfXG7JUubGHmC9hAU4zQX76nw0kuquOso130_provenance.
- NP83500.RAIEAf_HM91OJfXG7JUubGHmC9hAU4zQX76nw0kuquOso130_assertion wasDerivedFrom gad-20150221 NP83500.RAIEAf_HM91OJfXG7JUubGHmC9hAU4zQX76nw0kuquOso130_provenance.
- NP83500.RAIEAf_HM91OJfXG7JUubGHmC9hAU4zQX76nw0kuquOso130_assertion wasGeneratedBy ECO_0000203 NP83500.RAIEAf_HM91OJfXG7JUubGHmC9hAU4zQX76nw0kuquOso130_provenance.
- gad-20150221 importedOn "2015-02-21" NP83500.RAIEAf_HM91OJfXG7JUubGHmC9hAU4zQX76nw0kuquOso130_provenance.