Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP675487.RAo5cwTt-TV314SU7V5o79Cq-M2GIwbwuA7JQ6r4keXT0130_assertion> ?p ?o ?g. }
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- NP675487.RAo5cwTt-TV314SU7V5o79Cq-M2GIwbwuA7JQ6r4keXT0130_assertion type Assertion NP675487.RAo5cwTt-TV314SU7V5o79Cq-M2GIwbwuA7JQ6r4keXT0130_head.
- NP675487.RAo5cwTt-TV314SU7V5o79Cq-M2GIwbwuA7JQ6r4keXT0130_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." NP675487.RAo5cwTt-TV314SU7V5o79Cq-M2GIwbwuA7JQ6r4keXT0130_provenance.
- NP675487.RAo5cwTt-TV314SU7V5o79Cq-M2GIwbwuA7JQ6r4keXT0130_assertion evidence source_evidence_literature NP675487.RAo5cwTt-TV314SU7V5o79Cq-M2GIwbwuA7JQ6r4keXT0130_provenance.
- NP675487.RAo5cwTt-TV314SU7V5o79Cq-M2GIwbwuA7JQ6r4keXT0130_assertion SIO_000772 15389319 NP675487.RAo5cwTt-TV314SU7V5o79Cq-M2GIwbwuA7JQ6r4keXT0130_provenance.
- NP675487.RAo5cwTt-TV314SU7V5o79Cq-M2GIwbwuA7JQ6r4keXT0130_assertion wasDerivedFrom befree-20140225 NP675487.RAo5cwTt-TV314SU7V5o79Cq-M2GIwbwuA7JQ6r4keXT0130_provenance.
- NP675487.RAo5cwTt-TV314SU7V5o79Cq-M2GIwbwuA7JQ6r4keXT0130_assertion wasGeneratedBy ECO_0000203 NP675487.RAo5cwTt-TV314SU7V5o79Cq-M2GIwbwuA7JQ6r4keXT0130_provenance.