Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP815722.RAVMvlafz-VSO9uXgKYknUlsAX7ia6waApyWXmcAUhbIc130_assertion> ?p ?o ?g. }
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- NP815722.RAVMvlafz-VSO9uXgKYknUlsAX7ia6waApyWXmcAUhbIc130_assertion type Assertion NP815722.RAVMvlafz-VSO9uXgKYknUlsAX7ia6waApyWXmcAUhbIc130_head.
- NP815722.RAVMvlafz-VSO9uXgKYknUlsAX7ia6waApyWXmcAUhbIc130_assertion description "[Several different mutations in the KCNQ4 K+ channel gene are responsible for autosomal dominant nonsyndromic hearing impairment (DFNA2).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP815722.RAVMvlafz-VSO9uXgKYknUlsAX7ia6waApyWXmcAUhbIc130_provenance.
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- NP815722.RAVMvlafz-VSO9uXgKYknUlsAX7ia6waApyWXmcAUhbIc130_assertion SIO_000772 12112653 NP815722.RAVMvlafz-VSO9uXgKYknUlsAX7ia6waApyWXmcAUhbIc130_provenance.
- NP815722.RAVMvlafz-VSO9uXgKYknUlsAX7ia6waApyWXmcAUhbIc130_assertion wasDerivedFrom befree-20150227 NP815722.RAVMvlafz-VSO9uXgKYknUlsAX7ia6waApyWXmcAUhbIc130_provenance.
- NP815722.RAVMvlafz-VSO9uXgKYknUlsAX7ia6waApyWXmcAUhbIc130_assertion wasGeneratedBy ECO_0000203 NP815722.RAVMvlafz-VSO9uXgKYknUlsAX7ia6waApyWXmcAUhbIc130_provenance.