Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP3930.RAQGyq2UOmDr9K2cHH26oc7eo3hnMjBk3k9eZKu1tnZuk130_assertion> ?p ?o ?g. }
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- NP3930.RAQGyq2UOmDr9K2cHH26oc7eo3hnMjBk3k9eZKu1tnZuk130_assertion type Assertion NP3930.RAQGyq2UOmDr9K2cHH26oc7eo3hnMjBk3k9eZKu1tnZuk130_head.
- NP3930.RAQGyq2UOmDr9K2cHH26oc7eo3hnMjBk3k9eZKu1tnZuk130_assertion wasGeneratedBy ECO_0000218 NP3930.RAQGyq2UOmDr9K2cHH26oc7eo3hnMjBk3k9eZKu1tnZuk130_provenance.
- NP3930.RAQGyq2UOmDr9K2cHH26oc7eo3hnMjBk3k9eZKu1tnZuk130_assertion wasDerivedFrom uniprot-2016 NP3930.RAQGyq2UOmDr9K2cHH26oc7eo3hnMjBk3k9eZKu1tnZuk130_provenance.
- NP3930.RAQGyq2UOmDr9K2cHH26oc7eo3hnMjBk3k9eZKu1tnZuk130_assertion SIO_000772 15761194 NP3930.RAQGyq2UOmDr9K2cHH26oc7eo3hnMjBk3k9eZKu1tnZuk130_provenance.
- NP3930.RAQGyq2UOmDr9K2cHH26oc7eo3hnMjBk3k9eZKu1tnZuk130_assertion evidence source_evidence_curated NP3930.RAQGyq2UOmDr9K2cHH26oc7eo3hnMjBk3k9eZKu1tnZuk130_provenance.
- NP3930.RAQGyq2UOmDr9K2cHH26oc7eo3hnMjBk3k9eZKu1tnZuk130_assertion description "[A novel form of short QT syndrome (SQT3) is caused by a mutation in the KCNJ2 gene.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP3930.RAQGyq2UOmDr9K2cHH26oc7eo3hnMjBk3k9eZKu1tnZuk130_provenance.