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- NP293867.RAGtBIQdYwTTTo2ydUY2-6Z2rC91C7W6_3LgU0zqOs0wM130_assertion type Assertion NP293867.RAGtBIQdYwTTTo2ydUY2-6Z2rC91C7W6_3LgU0zqOs0wM130_head.
- NP293867.RAGtBIQdYwTTTo2ydUY2-6Z2rC91C7W6_3LgU0zqOs0wM130_assertion description "[Since Hey2 is one of the few Notch target genes, it is also conceivable that HEY2 mutations may account for cases of Alagille syndrome (AGS: variable combinations of heart, skeleton, eye, and facial malformations and cholestasis), in which the typical mutations of the Notch ligand JAG1 cannot be found.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP293867.RAGtBIQdYwTTTo2ydUY2-6Z2rC91C7W6_3LgU0zqOs0wM130_provenance.
- NP293867.RAGtBIQdYwTTTo2ydUY2-6Z2rC91C7W6_3LgU0zqOs0wM130_assertion evidence source_evidence_literature NP293867.RAGtBIQdYwTTTo2ydUY2-6Z2rC91C7W6_3LgU0zqOs0wM130_provenance.
- NP293867.RAGtBIQdYwTTTo2ydUY2-6Z2rC91C7W6_3LgU0zqOs0wM130_assertion SIO_000772 15389319 NP293867.RAGtBIQdYwTTTo2ydUY2-6Z2rC91C7W6_3LgU0zqOs0wM130_provenance.
- NP293867.RAGtBIQdYwTTTo2ydUY2-6Z2rC91C7W6_3LgU0zqOs0wM130_assertion wasDerivedFrom befree-20140225 NP293867.RAGtBIQdYwTTTo2ydUY2-6Z2rC91C7W6_3LgU0zqOs0wM130_provenance.
- NP293867.RAGtBIQdYwTTTo2ydUY2-6Z2rC91C7W6_3LgU0zqOs0wM130_assertion wasGeneratedBy ECO_0000203 NP293867.RAGtBIQdYwTTTo2ydUY2-6Z2rC91C7W6_3LgU0zqOs0wM130_provenance.