Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP647663.RAnlCoezZPYMVoVk5_y7clpAvlFmqVac8uzNrsiRz51rM130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP647663.RAnlCoezZPYMVoVk5_y7clpAvlFmqVac8uzNrsiRz51rM130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP647663.RAnlCoezZPYMVoVk5_y7clpAvlFmqVac8uzNrsiRz51rM130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP647663.RAnlCoezZPYMVoVk5_y7clpAvlFmqVac8uzNrsiRz51rM130_provenance.
- befree-2016 importedOn "2016-02-19" NP647663.RAnlCoezZPYMVoVk5_y7clpAvlFmqVac8uzNrsiRz51rM130_provenance.
- 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.