Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP805580.RAQ9Muq4yU434JttNGsKUpZy2CX8v4ns9cMW6NOE3rqmQ130_assertion> ?p ?o ?g. }
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- NP805580.RAQ9Muq4yU434JttNGsKUpZy2CX8v4ns9cMW6NOE3rqmQ130_assertion type Assertion NP805580.RAQ9Muq4yU434JttNGsKUpZy2CX8v4ns9cMW6NOE3rqmQ130_head.
- NP805580.RAQ9Muq4yU434JttNGsKUpZy2CX8v4ns9cMW6NOE3rqmQ130_assertion wasGeneratedBy ECO_0000203 NP805580.RAQ9Muq4yU434JttNGsKUpZy2CX8v4ns9cMW6NOE3rqmQ130_provenance.
- NP805580.RAQ9Muq4yU434JttNGsKUpZy2CX8v4ns9cMW6NOE3rqmQ130_assertion wasDerivedFrom befree-20140225 NP805580.RAQ9Muq4yU434JttNGsKUpZy2CX8v4ns9cMW6NOE3rqmQ130_provenance.
- NP805580.RAQ9Muq4yU434JttNGsKUpZy2CX8v4ns9cMW6NOE3rqmQ130_assertion SIO_000772 17646576 NP805580.RAQ9Muq4yU434JttNGsKUpZy2CX8v4ns9cMW6NOE3rqmQ130_provenance.
- NP805580.RAQ9Muq4yU434JttNGsKUpZy2CX8v4ns9cMW6NOE3rqmQ130_assertion evidence source_evidence_literature NP805580.RAQ9Muq4yU434JttNGsKUpZy2CX8v4ns9cMW6NOE3rqmQ130_provenance.
- NP805580.RAQ9Muq4yU434JttNGsKUpZy2CX8v4ns9cMW6NOE3rqmQ130_assertion description "[We describe an inherited, autosomal-dominant form of sinus node dysfunction caused by a missense mutation in the HCN4 ion channel pore.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP805580.RAQ9Muq4yU434JttNGsKUpZy2CX8v4ns9cMW6NOE3rqmQ130_provenance.