Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP461546.RAi9gRaTM4PeVUG2YY2hhxSrNFN2JF_kOZ4DKHMtl_d4A130_assertion> ?p ?o ?g. }
Showing items 1 to 6 of
6
with 100 items per page.
- NP461546.RAi9gRaTM4PeVUG2YY2hhxSrNFN2JF_kOZ4DKHMtl_d4A130_assertion type Assertion NP461546.RAi9gRaTM4PeVUG2YY2hhxSrNFN2JF_kOZ4DKHMtl_d4A130_head.
- NP461546.RAi9gRaTM4PeVUG2YY2hhxSrNFN2JF_kOZ4DKHMtl_d4A130_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." NP461546.RAi9gRaTM4PeVUG2YY2hhxSrNFN2JF_kOZ4DKHMtl_d4A130_provenance.
- NP461546.RAi9gRaTM4PeVUG2YY2hhxSrNFN2JF_kOZ4DKHMtl_d4A130_assertion evidence source_evidence_literature NP461546.RAi9gRaTM4PeVUG2YY2hhxSrNFN2JF_kOZ4DKHMtl_d4A130_provenance.
- NP461546.RAi9gRaTM4PeVUG2YY2hhxSrNFN2JF_kOZ4DKHMtl_d4A130_assertion SIO_000772 15389319 NP461546.RAi9gRaTM4PeVUG2YY2hhxSrNFN2JF_kOZ4DKHMtl_d4A130_provenance.
- NP461546.RAi9gRaTM4PeVUG2YY2hhxSrNFN2JF_kOZ4DKHMtl_d4A130_assertion wasDerivedFrom befree-2016 NP461546.RAi9gRaTM4PeVUG2YY2hhxSrNFN2JF_kOZ4DKHMtl_d4A130_provenance.
- NP461546.RAi9gRaTM4PeVUG2YY2hhxSrNFN2JF_kOZ4DKHMtl_d4A130_assertion wasGeneratedBy ECO_0000203 NP461546.RAi9gRaTM4PeVUG2YY2hhxSrNFN2JF_kOZ4DKHMtl_d4A130_provenance.