Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP35062.RAAyofWpTGCVYjmDlahLMZPLCbxt5Ody7p5tCLnofhs9o130_provenance>. }
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- source_evidence_curated type ECO_0000205 NP35062.RAAyofWpTGCVYjmDlahLMZPLCbxt5Ody7p5tCLnofhs9o130_provenance.
- source_evidence_curated label "DisGeNET evidence - CURATED" NP35062.RAAyofWpTGCVYjmDlahLMZPLCbxt5Ody7p5tCLnofhs9o130_provenance.
- source_evidence_curated comment "Gene-disease associations manually curated." NP35062.RAAyofWpTGCVYjmDlahLMZPLCbxt5Ody7p5tCLnofhs9o130_provenance.
- NP35062.RAAyofWpTGCVYjmDlahLMZPLCbxt5Ody7p5tCLnofhs9o130_assertion description "[Molecular basis of the dominant negative effect of a glycine transporter 2 mutation associated with hyperekplexia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP35062.RAAyofWpTGCVYjmDlahLMZPLCbxt5Ody7p5tCLnofhs9o130_provenance.
- NP35062.RAAyofWpTGCVYjmDlahLMZPLCbxt5Ody7p5tCLnofhs9o130_assertion evidence source_evidence_curated NP35062.RAAyofWpTGCVYjmDlahLMZPLCbxt5Ody7p5tCLnofhs9o130_provenance.
- NP35062.RAAyofWpTGCVYjmDlahLMZPLCbxt5Ody7p5tCLnofhs9o130_assertion SIO_000772 25480793 NP35062.RAAyofWpTGCVYjmDlahLMZPLCbxt5Ody7p5tCLnofhs9o130_provenance.
- NP35062.RAAyofWpTGCVYjmDlahLMZPLCbxt5Ody7p5tCLnofhs9o130_assertion wasDerivedFrom ctd_human-2016 NP35062.RAAyofWpTGCVYjmDlahLMZPLCbxt5Ody7p5tCLnofhs9o130_provenance.
- NP35062.RAAyofWpTGCVYjmDlahLMZPLCbxt5Ody7p5tCLnofhs9o130_assertion wasGeneratedBy ECO_0000218 NP35062.RAAyofWpTGCVYjmDlahLMZPLCbxt5Ody7p5tCLnofhs9o130_provenance.
- ctd_human-2016 importedOn "2016-01-25" NP35062.RAAyofWpTGCVYjmDlahLMZPLCbxt5Ody7p5tCLnofhs9o130_provenance.