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- NP522383.RANylSQ6SMJ0jKG4mTcdkH9Aeu8harMAxouuQ8JuwQT2I130_assertion type Assertion NP522383.RANylSQ6SMJ0jKG4mTcdkH9Aeu8harMAxouuQ8JuwQT2I130_head.
- NP522383.RANylSQ6SMJ0jKG4mTcdkH9Aeu8harMAxouuQ8JuwQT2I130_assertion wasGeneratedBy ECO_0000203 NP522383.RANylSQ6SMJ0jKG4mTcdkH9Aeu8harMAxouuQ8JuwQT2I130_provenance.
- NP522383.RANylSQ6SMJ0jKG4mTcdkH9Aeu8harMAxouuQ8JuwQT2I130_assertion wasDerivedFrom befree-20150227 NP522383.RANylSQ6SMJ0jKG4mTcdkH9Aeu8harMAxouuQ8JuwQT2I130_provenance.
- NP522383.RANylSQ6SMJ0jKG4mTcdkH9Aeu8harMAxouuQ8JuwQT2I130_assertion SIO_000772 15761194 NP522383.RANylSQ6SMJ0jKG4mTcdkH9Aeu8harMAxouuQ8JuwQT2I130_provenance.
- NP522383.RANylSQ6SMJ0jKG4mTcdkH9Aeu8harMAxouuQ8JuwQT2I130_assertion evidence source_evidence_literature NP522383.RANylSQ6SMJ0jKG4mTcdkH9Aeu8harMAxouuQ8JuwQT2I130_provenance.
- NP522383.RANylSQ6SMJ0jKG4mTcdkH9Aeu8harMAxouuQ8JuwQT2I130_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." NP522383.RANylSQ6SMJ0jKG4mTcdkH9Aeu8harMAxouuQ8JuwQT2I130_provenance.