Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP1170189.RAd9AEo7E_r_agn5KFKx2ijw3EFmMhkzkoFez6wV7qEOU130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP1170189.RAd9AEo7E_r_agn5KFKx2ijw3EFmMhkzkoFez6wV7qEOU130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP1170189.RAd9AEo7E_r_agn5KFKx2ijw3EFmMhkzkoFez6wV7qEOU130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP1170189.RAd9AEo7E_r_agn5KFKx2ijw3EFmMhkzkoFez6wV7qEOU130_provenance.
- NP1170189.RAd9AEo7E_r_agn5KFKx2ijw3EFmMhkzkoFez6wV7qEOU130_assertion description "[To identify the cause of childhood onset involuntary paroxysmal choreiform and dystonic movements in 2 unrelated sporadic cases and to investigate the functional effect of missense mutations in adenylyl cyclase 5 (ADCY5) in sporadic and inherited cases of autosomal dominant familial dyskinesia with facial myokymia (FDFM).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1170189.RAd9AEo7E_r_agn5KFKx2ijw3EFmMhkzkoFez6wV7qEOU130_provenance.
- NP1170189.RAd9AEo7E_r_agn5KFKx2ijw3EFmMhkzkoFez6wV7qEOU130_assertion evidence source_evidence_literature NP1170189.RAd9AEo7E_r_agn5KFKx2ijw3EFmMhkzkoFez6wV7qEOU130_provenance.
- NP1170189.RAd9AEo7E_r_agn5KFKx2ijw3EFmMhkzkoFez6wV7qEOU130_assertion SIO_000772 24700542 NP1170189.RAd9AEo7E_r_agn5KFKx2ijw3EFmMhkzkoFez6wV7qEOU130_provenance.
- NP1170189.RAd9AEo7E_r_agn5KFKx2ijw3EFmMhkzkoFez6wV7qEOU130_assertion wasDerivedFrom befree-2016 NP1170189.RAd9AEo7E_r_agn5KFKx2ijw3EFmMhkzkoFez6wV7qEOU130_provenance.
- NP1170189.RAd9AEo7E_r_agn5KFKx2ijw3EFmMhkzkoFez6wV7qEOU130_assertion wasGeneratedBy ECO_0000203 NP1170189.RAd9AEo7E_r_agn5KFKx2ijw3EFmMhkzkoFez6wV7qEOU130_provenance.
- befree-2016 importedOn "2016-02-19" NP1170189.RAd9AEo7E_r_agn5KFKx2ijw3EFmMhkzkoFez6wV7qEOU130_provenance.