Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP137980.RAZWbbdJJsxqk0Opj0W-GYm5WGaHQzNX9ECUe2NFb19H0130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP137980.RAZWbbdJJsxqk0Opj0W-GYm5WGaHQzNX9ECUe2NFb19H0130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP137980.RAZWbbdJJsxqk0Opj0W-GYm5WGaHQzNX9ECUe2NFb19H0130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP137980.RAZWbbdJJsxqk0Opj0W-GYm5WGaHQzNX9ECUe2NFb19H0130_provenance.
- NP137980.RAZWbbdJJsxqk0Opj0W-GYm5WGaHQzNX9ECUe2NFb19H0130_assertion description "[Further gene characterization and subtle mutations within the SMN1 gene need to be studied in order to define the molecular basis of SMA in the Chinese population.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP137980.RAZWbbdJJsxqk0Opj0W-GYm5WGaHQzNX9ECUe2NFb19H0130_provenance.
- NP137980.RAZWbbdJJsxqk0Opj0W-GYm5WGaHQzNX9ECUe2NFb19H0130_assertion evidence source_evidence_literature NP137980.RAZWbbdJJsxqk0Opj0W-GYm5WGaHQzNX9ECUe2NFb19H0130_provenance.
- NP137980.RAZWbbdJJsxqk0Opj0W-GYm5WGaHQzNX9ECUe2NFb19H0130_assertion SIO_000772 19134255 NP137980.RAZWbbdJJsxqk0Opj0W-GYm5WGaHQzNX9ECUe2NFb19H0130_provenance.
- NP137980.RAZWbbdJJsxqk0Opj0W-GYm5WGaHQzNX9ECUe2NFb19H0130_assertion wasDerivedFrom gad-20150221 NP137980.RAZWbbdJJsxqk0Opj0W-GYm5WGaHQzNX9ECUe2NFb19H0130_provenance.
- NP137980.RAZWbbdJJsxqk0Opj0W-GYm5WGaHQzNX9ECUe2NFb19H0130_assertion wasGeneratedBy ECO_0000203 NP137980.RAZWbbdJJsxqk0Opj0W-GYm5WGaHQzNX9ECUe2NFb19H0130_provenance.
- gad-20150221 importedOn "2015-02-21" NP137980.RAZWbbdJJsxqk0Opj0W-GYm5WGaHQzNX9ECUe2NFb19H0130_provenance.