Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP238.RAZE6EdPpIwbyaz_5X2e2uLtkjZx56gfawRERpVZZICao130_provenance>. }
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- source_evidence_curated type ECO_0000205 NP238.RAZE6EdPpIwbyaz_5X2e2uLtkjZx56gfawRERpVZZICao130_provenance.
- source_evidence_curated label "DisGeNET evidence - CURATED" NP238.RAZE6EdPpIwbyaz_5X2e2uLtkjZx56gfawRERpVZZICao130_provenance.
- source_evidence_curated comment "Gene-disease associations manually curated." NP238.RAZE6EdPpIwbyaz_5X2e2uLtkjZx56gfawRERpVZZICao130_provenance.
- NP238.RAZE6EdPpIwbyaz_5X2e2uLtkjZx56gfawRERpVZZICao130_assertion description "[Congenital long-QT syndrome caused by a novel mutation in a conserved acidic domain of the cardiac Na+ channel.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP238.RAZE6EdPpIwbyaz_5X2e2uLtkjZx56gfawRERpVZZICao130_provenance.
- NP238.RAZE6EdPpIwbyaz_5X2e2uLtkjZx56gfawRERpVZZICao130_assertion evidence source_evidence_curated NP238.RAZE6EdPpIwbyaz_5X2e2uLtkjZx56gfawRERpVZZICao130_provenance.
- NP238.RAZE6EdPpIwbyaz_5X2e2uLtkjZx56gfawRERpVZZICao130_assertion SIO_000772 10377081 NP238.RAZE6EdPpIwbyaz_5X2e2uLtkjZx56gfawRERpVZZICao130_provenance.
- NP238.RAZE6EdPpIwbyaz_5X2e2uLtkjZx56gfawRERpVZZICao130_assertion wasDerivedFrom uniprot-2016 NP238.RAZE6EdPpIwbyaz_5X2e2uLtkjZx56gfawRERpVZZICao130_provenance.
- NP238.RAZE6EdPpIwbyaz_5X2e2uLtkjZx56gfawRERpVZZICao130_assertion wasGeneratedBy ECO_0000218 NP238.RAZE6EdPpIwbyaz_5X2e2uLtkjZx56gfawRERpVZZICao130_provenance.
- uniprot-2016 importedOn "2016-01-25" NP238.RAZE6EdPpIwbyaz_5X2e2uLtkjZx56gfawRERpVZZICao130_provenance.