Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP1239591.RAYxzO3TB6WPi-PeO8KPTWViXYpXH9bP_43hQITAWeHLI130_assertion> ?p ?o ?g. }
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- NP1239591.RAYxzO3TB6WPi-PeO8KPTWViXYpXH9bP_43hQITAWeHLI130_assertion type Assertion NP1239591.RAYxzO3TB6WPi-PeO8KPTWViXYpXH9bP_43hQITAWeHLI130_head.
- NP1239591.RAYxzO3TB6WPi-PeO8KPTWViXYpXH9bP_43hQITAWeHLI130_assertion description "[When the particular phenotype of MFS includes a mutation on the RFX6 gene and neonatal diabetes, it has been called Mitchell-Riley syndrome.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1239591.RAYxzO3TB6WPi-PeO8KPTWViXYpXH9bP_43hQITAWeHLI130_provenance.
- NP1239591.RAYxzO3TB6WPi-PeO8KPTWViXYpXH9bP_43hQITAWeHLI130_assertion evidence source_evidence_literature NP1239591.RAYxzO3TB6WPi-PeO8KPTWViXYpXH9bP_43hQITAWeHLI130_provenance.
- NP1239591.RAYxzO3TB6WPi-PeO8KPTWViXYpXH9bP_43hQITAWeHLI130_assertion SIO_000772 25421130 NP1239591.RAYxzO3TB6WPi-PeO8KPTWViXYpXH9bP_43hQITAWeHLI130_provenance.
- NP1239591.RAYxzO3TB6WPi-PeO8KPTWViXYpXH9bP_43hQITAWeHLI130_assertion wasDerivedFrom befree-2016 NP1239591.RAYxzO3TB6WPi-PeO8KPTWViXYpXH9bP_43hQITAWeHLI130_provenance.
- NP1239591.RAYxzO3TB6WPi-PeO8KPTWViXYpXH9bP_43hQITAWeHLI130_assertion wasGeneratedBy ECO_0000203 NP1239591.RAYxzO3TB6WPi-PeO8KPTWViXYpXH9bP_43hQITAWeHLI130_provenance.