Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP3545.RA3pMdoi7kpQ28PshePRoDvPohJhxvX-QmZOi3x1nUZc8130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_curated type ECO_0000205 NP3545.RA3pMdoi7kpQ28PshePRoDvPohJhxvX-QmZOi3x1nUZc8130_provenance.
- source_evidence_curated label "DisGeNET evidence - CURATED" NP3545.RA3pMdoi7kpQ28PshePRoDvPohJhxvX-QmZOi3x1nUZc8130_provenance.
- source_evidence_curated comment "Gene-disease associations manually curated." NP3545.RA3pMdoi7kpQ28PshePRoDvPohJhxvX-QmZOi3x1nUZc8130_provenance.
- NP3545.RA3pMdoi7kpQ28PshePRoDvPohJhxvX-QmZOi3x1nUZc8130_assertion description "[A novel mutation in KCNQ2 associated with BFNC, drug resistant epilepsy, and mental retardation.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP3545.RA3pMdoi7kpQ28PshePRoDvPohJhxvX-QmZOi3x1nUZc8130_provenance.
- NP3545.RA3pMdoi7kpQ28PshePRoDvPohJhxvX-QmZOi3x1nUZc8130_assertion evidence source_evidence_curated NP3545.RA3pMdoi7kpQ28PshePRoDvPohJhxvX-QmZOi3x1nUZc8130_provenance.
- NP3545.RA3pMdoi7kpQ28PshePRoDvPohJhxvX-QmZOi3x1nUZc8130_assertion SIO_000772 15249611 NP3545.RA3pMdoi7kpQ28PshePRoDvPohJhxvX-QmZOi3x1nUZc8130_provenance.
- NP3545.RA3pMdoi7kpQ28PshePRoDvPohJhxvX-QmZOi3x1nUZc8130_assertion wasDerivedFrom uniprot-2016 NP3545.RA3pMdoi7kpQ28PshePRoDvPohJhxvX-QmZOi3x1nUZc8130_provenance.
- NP3545.RA3pMdoi7kpQ28PshePRoDvPohJhxvX-QmZOi3x1nUZc8130_assertion wasGeneratedBy ECO_0000218 NP3545.RA3pMdoi7kpQ28PshePRoDvPohJhxvX-QmZOi3x1nUZc8130_provenance.
- uniprot-2016 importedOn "2016-01-25" NP3545.RA3pMdoi7kpQ28PshePRoDvPohJhxvX-QmZOi3x1nUZc8130_provenance.