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- NP190425.RATC_8VedgX9wkjD_tNrcYjfK6RNkhgvSw9CP7OMDHvUc130_assertion type Assertion NP190425.RATC_8VedgX9wkjD_tNrcYjfK6RNkhgvSw9CP7OMDHvUc130_head.
- NP190425.RATC_8VedgX9wkjD_tNrcYjfK6RNkhgvSw9CP7OMDHvUc130_assertion wasGeneratedBy ECO_0000203 NP190425.RATC_8VedgX9wkjD_tNrcYjfK6RNkhgvSw9CP7OMDHvUc130_provenance.
- NP190425.RATC_8VedgX9wkjD_tNrcYjfK6RNkhgvSw9CP7OMDHvUc130_assertion wasDerivedFrom befree-20140225 NP190425.RATC_8VedgX9wkjD_tNrcYjfK6RNkhgvSw9CP7OMDHvUc130_provenance.
- NP190425.RATC_8VedgX9wkjD_tNrcYjfK6RNkhgvSw9CP7OMDHvUc130_assertion SIO_000772 10898405 NP190425.RATC_8VedgX9wkjD_tNrcYjfK6RNkhgvSw9CP7OMDHvUc130_provenance.
- NP190425.RATC_8VedgX9wkjD_tNrcYjfK6RNkhgvSw9CP7OMDHvUc130_assertion evidence source_evidence_literature NP190425.RATC_8VedgX9wkjD_tNrcYjfK6RNkhgvSw9CP7OMDHvUc130_provenance.
- NP190425.RATC_8VedgX9wkjD_tNrcYjfK6RNkhgvSw9CP7OMDHvUc130_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." NP190425.RATC_8VedgX9wkjD_tNrcYjfK6RNkhgvSw9CP7OMDHvUc130_provenance.