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- source_evidence_literature type ECO_0000212 NP815722.RAVMvlafz-VSO9uXgKYknUlsAX7ia6waApyWXmcAUhbIc130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP815722.RAVMvlafz-VSO9uXgKYknUlsAX7ia6waApyWXmcAUhbIc130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP815722.RAVMvlafz-VSO9uXgKYknUlsAX7ia6waApyWXmcAUhbIc130_provenance.
- 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.
- NP815722.RAVMvlafz-VSO9uXgKYknUlsAX7ia6waApyWXmcAUhbIc130_assertion evidence source_evidence_literature NP815722.RAVMvlafz-VSO9uXgKYknUlsAX7ia6waApyWXmcAUhbIc130_provenance.
- 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.
- befree-20150227 importedOn "2015-02-27" NP815722.RAVMvlafz-VSO9uXgKYknUlsAX7ia6waApyWXmcAUhbIc130_provenance.