Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP393089.RAtFXlvOSH4SWSxDaaQPnI-tTf7p-8hrXvRwO2yiCB8QQ130_assertion> ?p ?o ?g. }
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- NP393089.RAtFXlvOSH4SWSxDaaQPnI-tTf7p-8hrXvRwO2yiCB8QQ130_assertion type Assertion NP393089.RAtFXlvOSH4SWSxDaaQPnI-tTf7p-8hrXvRwO2yiCB8QQ130_head.
- NP393089.RAtFXlvOSH4SWSxDaaQPnI-tTf7p-8hrXvRwO2yiCB8QQ130_assertion description "[The PDS gene (7q31), responsible for Pendred syndrome (congenital sensorineural hearing loss and goiter), encodes a transmembrane protein known as pendrin.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP393089.RAtFXlvOSH4SWSxDaaQPnI-tTf7p-8hrXvRwO2yiCB8QQ130_provenance.
- NP393089.RAtFXlvOSH4SWSxDaaQPnI-tTf7p-8hrXvRwO2yiCB8QQ130_assertion evidence source_evidence_literature NP393089.RAtFXlvOSH4SWSxDaaQPnI-tTf7p-8hrXvRwO2yiCB8QQ130_provenance.
- NP393089.RAtFXlvOSH4SWSxDaaQPnI-tTf7p-8hrXvRwO2yiCB8QQ130_assertion SIO_000772 12727986 NP393089.RAtFXlvOSH4SWSxDaaQPnI-tTf7p-8hrXvRwO2yiCB8QQ130_provenance.
- NP393089.RAtFXlvOSH4SWSxDaaQPnI-tTf7p-8hrXvRwO2yiCB8QQ130_assertion wasDerivedFrom befree-2016 NP393089.RAtFXlvOSH4SWSxDaaQPnI-tTf7p-8hrXvRwO2yiCB8QQ130_provenance.
- NP393089.RAtFXlvOSH4SWSxDaaQPnI-tTf7p-8hrXvRwO2yiCB8QQ130_assertion wasGeneratedBy ECO_0000203 NP393089.RAtFXlvOSH4SWSxDaaQPnI-tTf7p-8hrXvRwO2yiCB8QQ130_provenance.