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- NP835205.RAmqfJWE6E09l0IMjprmX7ZjQRj2_ZBcBjEjy5gsCMGMQ130_assertion type Assertion NP835205.RAmqfJWE6E09l0IMjprmX7ZjQRj2_ZBcBjEjy5gsCMGMQ130_head.
- NP835205.RAmqfJWE6E09l0IMjprmX7ZjQRj2_ZBcBjEjy5gsCMGMQ130_assertion wasGeneratedBy ECO_0000203 NP835205.RAmqfJWE6E09l0IMjprmX7ZjQRj2_ZBcBjEjy5gsCMGMQ130_provenance.
- NP835205.RAmqfJWE6E09l0IMjprmX7ZjQRj2_ZBcBjEjy5gsCMGMQ130_assertion wasDerivedFrom befree-20150227 NP835205.RAmqfJWE6E09l0IMjprmX7ZjQRj2_ZBcBjEjy5gsCMGMQ130_provenance.
- NP835205.RAmqfJWE6E09l0IMjprmX7ZjQRj2_ZBcBjEjy5gsCMGMQ130_assertion SIO_000772 17646576 NP835205.RAmqfJWE6E09l0IMjprmX7ZjQRj2_ZBcBjEjy5gsCMGMQ130_provenance.
- NP835205.RAmqfJWE6E09l0IMjprmX7ZjQRj2_ZBcBjEjy5gsCMGMQ130_assertion evidence source_evidence_literature NP835205.RAmqfJWE6E09l0IMjprmX7ZjQRj2_ZBcBjEjy5gsCMGMQ130_provenance.
- NP835205.RAmqfJWE6E09l0IMjprmX7ZjQRj2_ZBcBjEjy5gsCMGMQ130_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." NP835205.RAmqfJWE6E09l0IMjprmX7ZjQRj2_ZBcBjEjy5gsCMGMQ130_provenance.