Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP1092465.RAS63Vi-NLP7-C35IEh2y2AZFjlf7sllzdyAbqeQrqdQY130_assertion> ?p ?o ?g. }
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- NP1092465.RAS63Vi-NLP7-C35IEh2y2AZFjlf7sllzdyAbqeQrqdQY130_assertion type Assertion NP1092465.RAS63Vi-NLP7-C35IEh2y2AZFjlf7sllzdyAbqeQrqdQY130_head.
- NP1092465.RAS63Vi-NLP7-C35IEh2y2AZFjlf7sllzdyAbqeQrqdQY130_assertion wasGeneratedBy ECO_0000203 NP1092465.RAS63Vi-NLP7-C35IEh2y2AZFjlf7sllzdyAbqeQrqdQY130_provenance.
- NP1092465.RAS63Vi-NLP7-C35IEh2y2AZFjlf7sllzdyAbqeQrqdQY130_assertion wasDerivedFrom befree-2016 NP1092465.RAS63Vi-NLP7-C35IEh2y2AZFjlf7sllzdyAbqeQrqdQY130_provenance.
- NP1092465.RAS63Vi-NLP7-C35IEh2y2AZFjlf7sllzdyAbqeQrqdQY130_assertion SIO_000772 23838540 NP1092465.RAS63Vi-NLP7-C35IEh2y2AZFjlf7sllzdyAbqeQrqdQY130_provenance.
- NP1092465.RAS63Vi-NLP7-C35IEh2y2AZFjlf7sllzdyAbqeQrqdQY130_assertion evidence source_evidence_literature NP1092465.RAS63Vi-NLP7-C35IEh2y2AZFjlf7sllzdyAbqeQrqdQY130_provenance.
- NP1092465.RAS63Vi-NLP7-C35IEh2y2AZFjlf7sllzdyAbqeQrqdQY130_assertion description "[A Novel mutation in the SLC26A4 gene in a Chinese family with Pendred syndrome.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1092465.RAS63Vi-NLP7-C35IEh2y2AZFjlf7sllzdyAbqeQrqdQY130_provenance.