Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP778436.RAOYEdbpJ5b5sYr-RSa_OZSqv-rtAQjBLUddjDaSxQlKQ130_assertion> ?p ?o ?g. }
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- NP778436.RAOYEdbpJ5b5sYr-RSa_OZSqv-rtAQjBLUddjDaSxQlKQ130_assertion type Assertion NP778436.RAOYEdbpJ5b5sYr-RSa_OZSqv-rtAQjBLUddjDaSxQlKQ130_head.
- NP778436.RAOYEdbpJ5b5sYr-RSa_OZSqv-rtAQjBLUddjDaSxQlKQ130_assertion description "[Mutations in JAG1 were detected in three patients with Alagille syndrome (1.3%), while NKX2.5 mutations were seen in two patients with non-syndromic ToF (0.9%).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP778436.RAOYEdbpJ5b5sYr-RSa_OZSqv-rtAQjBLUddjDaSxQlKQ130_provenance.
- NP778436.RAOYEdbpJ5b5sYr-RSa_OZSqv-rtAQjBLUddjDaSxQlKQ130_assertion evidence source_evidence_literature NP778436.RAOYEdbpJ5b5sYr-RSa_OZSqv-rtAQjBLUddjDaSxQlKQ130_provenance.
- NP778436.RAOYEdbpJ5b5sYr-RSa_OZSqv-rtAQjBLUddjDaSxQlKQ130_assertion SIO_000772 19948535 NP778436.RAOYEdbpJ5b5sYr-RSa_OZSqv-rtAQjBLUddjDaSxQlKQ130_provenance.
- NP778436.RAOYEdbpJ5b5sYr-RSa_OZSqv-rtAQjBLUddjDaSxQlKQ130_assertion wasDerivedFrom befree-2016 NP778436.RAOYEdbpJ5b5sYr-RSa_OZSqv-rtAQjBLUddjDaSxQlKQ130_provenance.
- NP778436.RAOYEdbpJ5b5sYr-RSa_OZSqv-rtAQjBLUddjDaSxQlKQ130_assertion wasGeneratedBy ECO_0000203 NP778436.RAOYEdbpJ5b5sYr-RSa_OZSqv-rtAQjBLUddjDaSxQlKQ130_provenance.