Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP393089.RAtFXlvOSH4SWSxDaaQPnI-tTf7p-8hrXvRwO2yiCB8QQ130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP393089.RAtFXlvOSH4SWSxDaaQPnI-tTf7p-8hrXvRwO2yiCB8QQ130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP393089.RAtFXlvOSH4SWSxDaaQPnI-tTf7p-8hrXvRwO2yiCB8QQ130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP393089.RAtFXlvOSH4SWSxDaaQPnI-tTf7p-8hrXvRwO2yiCB8QQ130_provenance.
- 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.
- befree-2016 importedOn "2016-02-19" NP393089.RAtFXlvOSH4SWSxDaaQPnI-tTf7p-8hrXvRwO2yiCB8QQ130_provenance.