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- source_evidence_literature type ECO_0000212 NP434517.RAmhNqtrTsIs6HeYvnHhzpJppznEcGwdndBjx7P_qBjcI130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP434517.RAmhNqtrTsIs6HeYvnHhzpJppznEcGwdndBjx7P_qBjcI130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP434517.RAmhNqtrTsIs6HeYvnHhzpJppznEcGwdndBjx7P_qBjcI130_provenance.
- NP434517.RAmhNqtrTsIs6HeYvnHhzpJppznEcGwdndBjx7P_qBjcI130_assertion description "[Here, we identified two de novo mutations in patients with sporadic SCZ in GRIN2A and one de novo mutation in GRIN2B in a patient with ASD.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP434517.RAmhNqtrTsIs6HeYvnHhzpJppznEcGwdndBjx7P_qBjcI130_provenance.
- NP434517.RAmhNqtrTsIs6HeYvnHhzpJppznEcGwdndBjx7P_qBjcI130_assertion evidence source_evidence_literature NP434517.RAmhNqtrTsIs6HeYvnHhzpJppznEcGwdndBjx7P_qBjcI130_provenance.
- NP434517.RAmhNqtrTsIs6HeYvnHhzpJppznEcGwdndBjx7P_qBjcI130_assertion SIO_000772 22833210 NP434517.RAmhNqtrTsIs6HeYvnHhzpJppznEcGwdndBjx7P_qBjcI130_provenance.
- NP434517.RAmhNqtrTsIs6HeYvnHhzpJppznEcGwdndBjx7P_qBjcI130_assertion wasDerivedFrom befree-20150227 NP434517.RAmhNqtrTsIs6HeYvnHhzpJppznEcGwdndBjx7P_qBjcI130_provenance.
- NP434517.RAmhNqtrTsIs6HeYvnHhzpJppznEcGwdndBjx7P_qBjcI130_assertion wasGeneratedBy ECO_0000203 NP434517.RAmhNqtrTsIs6HeYvnHhzpJppznEcGwdndBjx7P_qBjcI130_provenance.
- befree-20150227 importedOn "2015-02-27" NP434517.RAmhNqtrTsIs6HeYvnHhzpJppznEcGwdndBjx7P_qBjcI130_provenance.