Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP647663.RAnlCoezZPYMVoVk5_y7clpAvlFmqVac8uzNrsiRz51rM130_assertion> ?p ?o ?g. }
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- NP647663.RAnlCoezZPYMVoVk5_y7clpAvlFmqVac8uzNrsiRz51rM130_assertion type Assertion NP647663.RAnlCoezZPYMVoVk5_y7clpAvlFmqVac8uzNrsiRz51rM130_head.
- NP647663.RAnlCoezZPYMVoVk5_y7clpAvlFmqVac8uzNrsiRz51rM130_assertion wasGeneratedBy ECO_0000203 NP647663.RAnlCoezZPYMVoVk5_y7clpAvlFmqVac8uzNrsiRz51rM130_provenance.
- NP647663.RAnlCoezZPYMVoVk5_y7clpAvlFmqVac8uzNrsiRz51rM130_assertion wasDerivedFrom befree-2016 NP647663.RAnlCoezZPYMVoVk5_y7clpAvlFmqVac8uzNrsiRz51rM130_provenance.
- NP647663.RAnlCoezZPYMVoVk5_y7clpAvlFmqVac8uzNrsiRz51rM130_assertion SIO_000772 18165683 NP647663.RAnlCoezZPYMVoVk5_y7clpAvlFmqVac8uzNrsiRz51rM130_provenance.
- NP647663.RAnlCoezZPYMVoVk5_y7clpAvlFmqVac8uzNrsiRz51rM130_assertion evidence source_evidence_literature NP647663.RAnlCoezZPYMVoVk5_y7clpAvlFmqVac8uzNrsiRz51rM130_provenance.
- NP647663.RAnlCoezZPYMVoVk5_y7clpAvlFmqVac8uzNrsiRz51rM130_assertion description "[KCNQ1 (Kv7.1), the founding subfamily member, encodes a channel subunit directly implicated in genetic disorders, such as the long QT syndrome, a cardiac pathology responsible for arrhythmias.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP647663.RAnlCoezZPYMVoVk5_y7clpAvlFmqVac8uzNrsiRz51rM130_provenance.