Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP865816.RAAbpcO8NV2L2a7wv0L-_3LHly-YTtSHdGo3ZpbCOIWO8130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP865816.RAAbpcO8NV2L2a7wv0L-_3LHly-YTtSHdGo3ZpbCOIWO8130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP865816.RAAbpcO8NV2L2a7wv0L-_3LHly-YTtSHdGo3ZpbCOIWO8130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP865816.RAAbpcO8NV2L2a7wv0L-_3LHly-YTtSHdGo3ZpbCOIWO8130_provenance.
- befree-2016 importedOn "2016-02-19" NP865816.RAAbpcO8NV2L2a7wv0L-_3LHly-YTtSHdGo3ZpbCOIWO8130_provenance.
- NP865816.RAAbpcO8NV2L2a7wv0L-_3LHly-YTtSHdGo3ZpbCOIWO8130_assertion wasGeneratedBy ECO_0000203 NP865816.RAAbpcO8NV2L2a7wv0L-_3LHly-YTtSHdGo3ZpbCOIWO8130_provenance.
- NP865816.RAAbpcO8NV2L2a7wv0L-_3LHly-YTtSHdGo3ZpbCOIWO8130_assertion wasDerivedFrom befree-2016 NP865816.RAAbpcO8NV2L2a7wv0L-_3LHly-YTtSHdGo3ZpbCOIWO8130_provenance.
- NP865816.RAAbpcO8NV2L2a7wv0L-_3LHly-YTtSHdGo3ZpbCOIWO8130_assertion SIO_000772 21241800 NP865816.RAAbpcO8NV2L2a7wv0L-_3LHly-YTtSHdGo3ZpbCOIWO8130_provenance.
- NP865816.RAAbpcO8NV2L2a7wv0L-_3LHly-YTtSHdGo3ZpbCOIWO8130_assertion evidence source_evidence_literature NP865816.RAAbpcO8NV2L2a7wv0L-_3LHly-YTtSHdGo3ZpbCOIWO8130_provenance.
- NP865816.RAAbpcO8NV2L2a7wv0L-_3LHly-YTtSHdGo3ZpbCOIWO8130_assertion description "[Biophysical properties of mutant KCNQ1 S277L channels linked to hereditary long QT syndrome with phenotypic variability.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP865816.RAAbpcO8NV2L2a7wv0L-_3LHly-YTtSHdGo3ZpbCOIWO8130_provenance.