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- source_evidence_literature type ECO_0000212 NP478474.RAaND_Sl1dbt6FyZzXf4Cn7o7fNLUO-31g_O28qF6XevM130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP478474.RAaND_Sl1dbt6FyZzXf4Cn7o7fNLUO-31g_O28qF6XevM130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP478474.RAaND_Sl1dbt6FyZzXf4Cn7o7fNLUO-31g_O28qF6XevM130_provenance.
- NP478474.RAaND_Sl1dbt6FyZzXf4Cn7o7fNLUO-31g_O28qF6XevM130_assertion description "[We screened the most common LRRK2 mutation (p.G2019S) in a series of 180 consecutive patients clinically diagnosed with Alzheimer Disease (AD).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP478474.RAaND_Sl1dbt6FyZzXf4Cn7o7fNLUO-31g_O28qF6XevM130_provenance.
- NP478474.RAaND_Sl1dbt6FyZzXf4Cn7o7fNLUO-31g_O28qF6XevM130_assertion evidence source_evidence_literature NP478474.RAaND_Sl1dbt6FyZzXf4Cn7o7fNLUO-31g_O28qF6XevM130_provenance.
- NP478474.RAaND_Sl1dbt6FyZzXf4Cn7o7fNLUO-31g_O28qF6XevM130_assertion SIO_000772 19822953 NP478474.RAaND_Sl1dbt6FyZzXf4Cn7o7fNLUO-31g_O28qF6XevM130_provenance.
- NP478474.RAaND_Sl1dbt6FyZzXf4Cn7o7fNLUO-31g_O28qF6XevM130_assertion wasDerivedFrom befree-20140225 NP478474.RAaND_Sl1dbt6FyZzXf4Cn7o7fNLUO-31g_O28qF6XevM130_provenance.
- NP478474.RAaND_Sl1dbt6FyZzXf4Cn7o7fNLUO-31g_O28qF6XevM130_assertion wasGeneratedBy ECO_0000203 NP478474.RAaND_Sl1dbt6FyZzXf4Cn7o7fNLUO-31g_O28qF6XevM130_provenance.
- befree-20140225 importedOn "2014-02-25" NP478474.RAaND_Sl1dbt6FyZzXf4Cn7o7fNLUO-31g_O28qF6XevM130_provenance.