Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP727864.RArd88yqbKhcc-1xBTlrF9OytfgkWuR1sqyiNzdNT0ZT4130_assertion> ?p ?o ?g. }
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- NP727864.RArd88yqbKhcc-1xBTlrF9OytfgkWuR1sqyiNzdNT0ZT4130_assertion type Assertion NP727864.RArd88yqbKhcc-1xBTlrF9OytfgkWuR1sqyiNzdNT0ZT4130_head.
- NP727864.RArd88yqbKhcc-1xBTlrF9OytfgkWuR1sqyiNzdNT0ZT4130_assertion wasGeneratedBy ECO_0000203 NP727864.RArd88yqbKhcc-1xBTlrF9OytfgkWuR1sqyiNzdNT0ZT4130_provenance.
- NP727864.RArd88yqbKhcc-1xBTlrF9OytfgkWuR1sqyiNzdNT0ZT4130_assertion wasDerivedFrom befree-20140225 NP727864.RArd88yqbKhcc-1xBTlrF9OytfgkWuR1sqyiNzdNT0ZT4130_provenance.
- NP727864.RArd88yqbKhcc-1xBTlrF9OytfgkWuR1sqyiNzdNT0ZT4130_assertion SIO_000772 10898405 NP727864.RArd88yqbKhcc-1xBTlrF9OytfgkWuR1sqyiNzdNT0ZT4130_provenance.
- NP727864.RArd88yqbKhcc-1xBTlrF9OytfgkWuR1sqyiNzdNT0ZT4130_assertion evidence source_evidence_literature NP727864.RArd88yqbKhcc-1xBTlrF9OytfgkWuR1sqyiNzdNT0ZT4130_provenance.
- NP727864.RArd88yqbKhcc-1xBTlrF9OytfgkWuR1sqyiNzdNT0ZT4130_assertion description "[It is becoming clear that mutations in the KVLQT1, human `ether-a-go-go` related gene, cardiac voltage-dependent sodium channel gene, minK and MiRP1 genes, respectively, are responsible for the LQT1, LQT2, LQT3, LQT5 and LQT6 variants of the Romano-Ward syndrome, characterized by autosomal dominant transmission and no deafness.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP727864.RArd88yqbKhcc-1xBTlrF9OytfgkWuR1sqyiNzdNT0ZT4130_provenance.