Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP532484.RA5lBEvg89SH7Yklo3BV1eP_OFl-YqJgVJLcvWnJNdJjU130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP532484.RA5lBEvg89SH7Yklo3BV1eP_OFl-YqJgVJLcvWnJNdJjU130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP532484.RA5lBEvg89SH7Yklo3BV1eP_OFl-YqJgVJLcvWnJNdJjU130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP532484.RA5lBEvg89SH7Yklo3BV1eP_OFl-YqJgVJLcvWnJNdJjU130_provenance.
- NP532484.RA5lBEvg89SH7Yklo3BV1eP_OFl-YqJgVJLcvWnJNdJjU130_assertion description "[This is the first study to identify a dominant mechanism, class 2, for the loss of Kv11.1 channel function in LQT2 and to report that the class 2 phenotype for many of these mutant channels can be corrected.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP532484.RA5lBEvg89SH7Yklo3BV1eP_OFl-YqJgVJLcvWnJNdJjU130_provenance.
- NP532484.RA5lBEvg89SH7Yklo3BV1eP_OFl-YqJgVJLcvWnJNdJjU130_assertion evidence source_evidence_literature NP532484.RA5lBEvg89SH7Yklo3BV1eP_OFl-YqJgVJLcvWnJNdJjU130_provenance.
- NP532484.RA5lBEvg89SH7Yklo3BV1eP_OFl-YqJgVJLcvWnJNdJjU130_assertion SIO_000772 16432067 NP532484.RA5lBEvg89SH7Yklo3BV1eP_OFl-YqJgVJLcvWnJNdJjU130_provenance.
- NP532484.RA5lBEvg89SH7Yklo3BV1eP_OFl-YqJgVJLcvWnJNdJjU130_assertion wasDerivedFrom befree-2016 NP532484.RA5lBEvg89SH7Yklo3BV1eP_OFl-YqJgVJLcvWnJNdJjU130_provenance.
- NP532484.RA5lBEvg89SH7Yklo3BV1eP_OFl-YqJgVJLcvWnJNdJjU130_assertion wasGeneratedBy ECO_0000203 NP532484.RA5lBEvg89SH7Yklo3BV1eP_OFl-YqJgVJLcvWnJNdJjU130_provenance.
- befree-2016 importedOn "2016-02-19" NP532484.RA5lBEvg89SH7Yklo3BV1eP_OFl-YqJgVJLcvWnJNdJjU130_provenance.