Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP479378.RA7rLcufNkEJKall2WEJWuiYX-S1qsP2PCoDXh-uUlO5U130_assertion> ?p ?o ?g. }
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- NP479378.RA7rLcufNkEJKall2WEJWuiYX-S1qsP2PCoDXh-uUlO5U130_assertion type Assertion NP479378.RA7rLcufNkEJKall2WEJWuiYX-S1qsP2PCoDXh-uUlO5U130_head.
- NP479378.RA7rLcufNkEJKall2WEJWuiYX-S1qsP2PCoDXh-uUlO5U130_assertion description "[Mutations in KVLQT1 and KCNE1 also cause the Jervell and Lange-Nielsen syndrome, a form of LQTS associated with deafness, a phenotypic abnormality inherited in an autosomal recessive fashion.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP479378.RA7rLcufNkEJKall2WEJWuiYX-S1qsP2PCoDXh-uUlO5U130_provenance.
- NP479378.RA7rLcufNkEJKall2WEJWuiYX-S1qsP2PCoDXh-uUlO5U130_assertion evidence source_evidence_literature NP479378.RA7rLcufNkEJKall2WEJWuiYX-S1qsP2PCoDXh-uUlO5U130_provenance.
- NP479378.RA7rLcufNkEJKall2WEJWuiYX-S1qsP2PCoDXh-uUlO5U130_assertion SIO_000772 10973849 NP479378.RA7rLcufNkEJKall2WEJWuiYX-S1qsP2PCoDXh-uUlO5U130_provenance.
- NP479378.RA7rLcufNkEJKall2WEJWuiYX-S1qsP2PCoDXh-uUlO5U130_assertion wasDerivedFrom befree-20140225 NP479378.RA7rLcufNkEJKall2WEJWuiYX-S1qsP2PCoDXh-uUlO5U130_provenance.
- NP479378.RA7rLcufNkEJKall2WEJWuiYX-S1qsP2PCoDXh-uUlO5U130_assertion wasGeneratedBy ECO_0000203 NP479378.RA7rLcufNkEJKall2WEJWuiYX-S1qsP2PCoDXh-uUlO5U130_provenance.