Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP580041.RADkqDTjqnHtzb3eNWP3-46FyrlAtJZFXMcWJUHphNNDg130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP580041.RADkqDTjqnHtzb3eNWP3-46FyrlAtJZFXMcWJUHphNNDg130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP580041.RADkqDTjqnHtzb3eNWP3-46FyrlAtJZFXMcWJUHphNNDg130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP580041.RADkqDTjqnHtzb3eNWP3-46FyrlAtJZFXMcWJUHphNNDg130_provenance.
- NP580041.RADkqDTjqnHtzb3eNWP3-46FyrlAtJZFXMcWJUHphNNDg130_assertion description "[Thus, the hyperekplexia phenotype of Glra1(D80A) mice is due to the loss of Zn(2+) potentiation of alpha1 subunit containing GlyRs, indicating that synaptic Zn(2+) is essential for proper in vivo functioning of glycinergic neurotransmission.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP580041.RADkqDTjqnHtzb3eNWP3-46FyrlAtJZFXMcWJUHphNNDg130_provenance.
- NP580041.RADkqDTjqnHtzb3eNWP3-46FyrlAtJZFXMcWJUHphNNDg130_assertion evidence source_evidence_literature NP580041.RADkqDTjqnHtzb3eNWP3-46FyrlAtJZFXMcWJUHphNNDg130_provenance.
- NP580041.RADkqDTjqnHtzb3eNWP3-46FyrlAtJZFXMcWJUHphNNDg130_assertion SIO_000772 17114051 NP580041.RADkqDTjqnHtzb3eNWP3-46FyrlAtJZFXMcWJUHphNNDg130_provenance.
- NP580041.RADkqDTjqnHtzb3eNWP3-46FyrlAtJZFXMcWJUHphNNDg130_assertion wasDerivedFrom befree-2016 NP580041.RADkqDTjqnHtzb3eNWP3-46FyrlAtJZFXMcWJUHphNNDg130_provenance.
- NP580041.RADkqDTjqnHtzb3eNWP3-46FyrlAtJZFXMcWJUHphNNDg130_assertion wasGeneratedBy ECO_0000203 NP580041.RADkqDTjqnHtzb3eNWP3-46FyrlAtJZFXMcWJUHphNNDg130_provenance.
- befree-2016 importedOn "2016-02-19" NP580041.RADkqDTjqnHtzb3eNWP3-46FyrlAtJZFXMcWJUHphNNDg130_provenance.