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- source_evidence_literature type ECO_0000212 NP1216776.RADVIPisE9OIF2ifShghX1YDz43igZlCHygwsyWxzHskM130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP1216776.RADVIPisE9OIF2ifShghX1YDz43igZlCHygwsyWxzHskM130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP1216776.RADVIPisE9OIF2ifShghX1YDz43igZlCHygwsyWxzHskM130_provenance.
- NP1216776.RADVIPisE9OIF2ifShghX1YDz43igZlCHygwsyWxzHskM130_assertion description "[A somatic GNAQ mutation was recently identified in patients with sporadic PWSs and Sturge-Weber syndrome.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1216776.RADVIPisE9OIF2ifShghX1YDz43igZlCHygwsyWxzHskM130_provenance.
- NP1216776.RADVIPisE9OIF2ifShghX1YDz43igZlCHygwsyWxzHskM130_assertion evidence source_evidence_literature NP1216776.RADVIPisE9OIF2ifShghX1YDz43igZlCHygwsyWxzHskM130_provenance.
- NP1216776.RADVIPisE9OIF2ifShghX1YDz43igZlCHygwsyWxzHskM130_assertion SIO_000772 25188413 NP1216776.RADVIPisE9OIF2ifShghX1YDz43igZlCHygwsyWxzHskM130_provenance.
- NP1216776.RADVIPisE9OIF2ifShghX1YDz43igZlCHygwsyWxzHskM130_assertion wasDerivedFrom befree-2016 NP1216776.RADVIPisE9OIF2ifShghX1YDz43igZlCHygwsyWxzHskM130_provenance.
- NP1216776.RADVIPisE9OIF2ifShghX1YDz43igZlCHygwsyWxzHskM130_assertion wasGeneratedBy ECO_0000203 NP1216776.RADVIPisE9OIF2ifShghX1YDz43igZlCHygwsyWxzHskM130_provenance.
- befree-2016 importedOn "2016-02-19" NP1216776.RADVIPisE9OIF2ifShghX1YDz43igZlCHygwsyWxzHskM130_provenance.