Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP6950.RAWpoF1fyTCEZTxxGUpQ45nRbFZl4Ulhea3b0B_VaB0hM130_provenance>. }
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- source_evidence_curated type ECO_0000205 NP6950.RAWpoF1fyTCEZTxxGUpQ45nRbFZl4Ulhea3b0B_VaB0hM130_provenance.
- source_evidence_curated label "DisGeNET evidence - CURATED" NP6950.RAWpoF1fyTCEZTxxGUpQ45nRbFZl4Ulhea3b0B_VaB0hM130_provenance.
- source_evidence_curated comment "Gene-disease associations manually curated." NP6950.RAWpoF1fyTCEZTxxGUpQ45nRbFZl4Ulhea3b0B_VaB0hM130_provenance.
- uniprot-2016 importedOn "2016-01-25" NP6950.RAWpoF1fyTCEZTxxGUpQ45nRbFZl4Ulhea3b0B_VaB0hM130_provenance.
- NP6950.RAWpoF1fyTCEZTxxGUpQ45nRbFZl4Ulhea3b0B_VaB0hM130_assertion wasGeneratedBy ECO_0000218 NP6950.RAWpoF1fyTCEZTxxGUpQ45nRbFZl4Ulhea3b0B_VaB0hM130_provenance.
- NP6950.RAWpoF1fyTCEZTxxGUpQ45nRbFZl4Ulhea3b0B_VaB0hM130_assertion wasDerivedFrom uniprot-2016 NP6950.RAWpoF1fyTCEZTxxGUpQ45nRbFZl4Ulhea3b0B_VaB0hM130_provenance.
- NP6950.RAWpoF1fyTCEZTxxGUpQ45nRbFZl4Ulhea3b0B_VaB0hM130_assertion SIO_000772 22314138 NP6950.RAWpoF1fyTCEZTxxGUpQ45nRbFZl4Ulhea3b0B_VaB0hM130_provenance.
- NP6950.RAWpoF1fyTCEZTxxGUpQ45nRbFZl4Ulhea3b0B_VaB0hM130_assertion evidence source_evidence_curated NP6950.RAWpoF1fyTCEZTxxGUpQ45nRbFZl4Ulhea3b0B_VaB0hM130_provenance.
- NP6950.RAWpoF1fyTCEZTxxGUpQ45nRbFZl4Ulhea3b0B_VaB0hM130_assertion description "[Identification and functional characterization of the novel human ether-a-go-go-related gene (hERG) R744P mutant associated with hereditary long QT syndrome 2.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP6950.RAWpoF1fyTCEZTxxGUpQ45nRbFZl4Ulhea3b0B_VaB0hM130_provenance.