Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP289262.RAjzlTt-K3aptsYF_l2nt_3KoN_x8YG7irkJaOV-l7nKQ130_assertion> ?p ?o ?g. }
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- NP289262.RAjzlTt-K3aptsYF_l2nt_3KoN_x8YG7irkJaOV-l7nKQ130_assertion type Assertion NP289262.RAjzlTt-K3aptsYF_l2nt_3KoN_x8YG7irkJaOV-l7nKQ130_head.
- NP289262.RAjzlTt-K3aptsYF_l2nt_3KoN_x8YG7irkJaOV-l7nKQ130_assertion wasGeneratedBy ECO_0000203 NP289262.RAjzlTt-K3aptsYF_l2nt_3KoN_x8YG7irkJaOV-l7nKQ130_provenance.
- NP289262.RAjzlTt-K3aptsYF_l2nt_3KoN_x8YG7irkJaOV-l7nKQ130_assertion wasDerivedFrom befree-2016 NP289262.RAjzlTt-K3aptsYF_l2nt_3KoN_x8YG7irkJaOV-l7nKQ130_provenance.
- NP289262.RAjzlTt-K3aptsYF_l2nt_3KoN_x8YG7irkJaOV-l7nKQ130_assertion SIO_000772 10898405 NP289262.RAjzlTt-K3aptsYF_l2nt_3KoN_x8YG7irkJaOV-l7nKQ130_provenance.
- NP289262.RAjzlTt-K3aptsYF_l2nt_3KoN_x8YG7irkJaOV-l7nKQ130_assertion evidence source_evidence_literature NP289262.RAjzlTt-K3aptsYF_l2nt_3KoN_x8YG7irkJaOV-l7nKQ130_provenance.
- NP289262.RAjzlTt-K3aptsYF_l2nt_3KoN_x8YG7irkJaOV-l7nKQ130_assertion description "[The much rarer Jervell-Lange-Nielsen syndrome (with marked QT prolongation and sensorineural deafness) arises when a child inherits mutant KVLQT1 or minK alleles from both parents.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP289262.RAjzlTt-K3aptsYF_l2nt_3KoN_x8YG7irkJaOV-l7nKQ130_provenance.