Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP498985.RAFRHkSbibjRrqFgdg7NlV65oI1ZdA2bYHXnOyfEmbwLE130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP498985.RAFRHkSbibjRrqFgdg7NlV65oI1ZdA2bYHXnOyfEmbwLE130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP498985.RAFRHkSbibjRrqFgdg7NlV65oI1ZdA2bYHXnOyfEmbwLE130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP498985.RAFRHkSbibjRrqFgdg7NlV65oI1ZdA2bYHXnOyfEmbwLE130_provenance.
- NP498985.RAFRHkSbibjRrqFgdg7NlV65oI1ZdA2bYHXnOyfEmbwLE130_assertion description "[This study highlights the functional relevance of the truncated KCNQ1 splice variant (isoform 2) in establishment and mode of inheritance in long QT syndrome.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP498985.RAFRHkSbibjRrqFgdg7NlV65oI1ZdA2bYHXnOyfEmbwLE130_provenance.
- NP498985.RAFRHkSbibjRrqFgdg7NlV65oI1ZdA2bYHXnOyfEmbwLE130_assertion evidence source_evidence_literature NP498985.RAFRHkSbibjRrqFgdg7NlV65oI1ZdA2bYHXnOyfEmbwLE130_provenance.
- NP498985.RAFRHkSbibjRrqFgdg7NlV65oI1ZdA2bYHXnOyfEmbwLE130_assertion SIO_000772 15950200 NP498985.RAFRHkSbibjRrqFgdg7NlV65oI1ZdA2bYHXnOyfEmbwLE130_provenance.
- NP498985.RAFRHkSbibjRrqFgdg7NlV65oI1ZdA2bYHXnOyfEmbwLE130_assertion wasDerivedFrom befree-2016 NP498985.RAFRHkSbibjRrqFgdg7NlV65oI1ZdA2bYHXnOyfEmbwLE130_provenance.
- NP498985.RAFRHkSbibjRrqFgdg7NlV65oI1ZdA2bYHXnOyfEmbwLE130_assertion wasGeneratedBy ECO_0000203 NP498985.RAFRHkSbibjRrqFgdg7NlV65oI1ZdA2bYHXnOyfEmbwLE130_provenance.
- befree-2016 importedOn "2016-02-19" NP498985.RAFRHkSbibjRrqFgdg7NlV65oI1ZdA2bYHXnOyfEmbwLE130_provenance.