Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP658374.RABvZ-GWZkXJmBXET1OrKJhl_QQt0W7r0ryxnkSvfH1UE130_assertion> ?p ?o ?g. }
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- NP658374.RABvZ-GWZkXJmBXET1OrKJhl_QQt0W7r0ryxnkSvfH1UE130_assertion type Assertion NP658374.RABvZ-GWZkXJmBXET1OrKJhl_QQt0W7r0ryxnkSvfH1UE130_head.
- NP658374.RABvZ-GWZkXJmBXET1OrKJhl_QQt0W7r0ryxnkSvfH1UE130_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." NP658374.RABvZ-GWZkXJmBXET1OrKJhl_QQt0W7r0ryxnkSvfH1UE130_provenance.
- NP658374.RABvZ-GWZkXJmBXET1OrKJhl_QQt0W7r0ryxnkSvfH1UE130_assertion evidence source_evidence_literature NP658374.RABvZ-GWZkXJmBXET1OrKJhl_QQt0W7r0ryxnkSvfH1UE130_provenance.
- NP658374.RABvZ-GWZkXJmBXET1OrKJhl_QQt0W7r0ryxnkSvfH1UE130_assertion SIO_000772 15389319 NP658374.RABvZ-GWZkXJmBXET1OrKJhl_QQt0W7r0ryxnkSvfH1UE130_provenance.
- NP658374.RABvZ-GWZkXJmBXET1OrKJhl_QQt0W7r0ryxnkSvfH1UE130_assertion wasDerivedFrom befree-20140225 NP658374.RABvZ-GWZkXJmBXET1OrKJhl_QQt0W7r0ryxnkSvfH1UE130_provenance.
- NP658374.RABvZ-GWZkXJmBXET1OrKJhl_QQt0W7r0ryxnkSvfH1UE130_assertion wasGeneratedBy ECO_0000203 NP658374.RABvZ-GWZkXJmBXET1OrKJhl_QQt0W7r0ryxnkSvfH1UE130_provenance.