Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP134661.RANeFNOFZT8ViqbSkhcuzcM2oGDpN1ooxbPl8CXbei1ts130_assertion> ?p ?o ?g. }
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- NP134661.RANeFNOFZT8ViqbSkhcuzcM2oGDpN1ooxbPl8CXbei1ts130_assertion type Assertion NP134661.RANeFNOFZT8ViqbSkhcuzcM2oGDpN1ooxbPl8CXbei1ts130_head.
- NP134661.RANeFNOFZT8ViqbSkhcuzcM2oGDpN1ooxbPl8CXbei1ts130_assertion wasGeneratedBy ECO_0000203 NP134661.RANeFNOFZT8ViqbSkhcuzcM2oGDpN1ooxbPl8CXbei1ts130_provenance.
- NP134661.RANeFNOFZT8ViqbSkhcuzcM2oGDpN1ooxbPl8CXbei1ts130_assertion wasDerivedFrom gad-20150221 NP134661.RANeFNOFZT8ViqbSkhcuzcM2oGDpN1ooxbPl8CXbei1ts130_provenance.
- NP134661.RANeFNOFZT8ViqbSkhcuzcM2oGDpN1ooxbPl8CXbei1ts130_assertion SIO_000772 19027966 NP134661.RANeFNOFZT8ViqbSkhcuzcM2oGDpN1ooxbPl8CXbei1ts130_provenance.
- NP134661.RANeFNOFZT8ViqbSkhcuzcM2oGDpN1ooxbPl8CXbei1ts130_assertion evidence source_evidence_literature NP134661.RANeFNOFZT8ViqbSkhcuzcM2oGDpN1ooxbPl8CXbei1ts130_provenance.
- NP134661.RANeFNOFZT8ViqbSkhcuzcM2oGDpN1ooxbPl8CXbei1ts130_assertion description "[Splice variant IVS2-2A>G in the SLC26A5 (Prestin) gene in five Estonian families with hearing loss.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP134661.RANeFNOFZT8ViqbSkhcuzcM2oGDpN1ooxbPl8CXbei1ts130_provenance.