Nanopublications LDF server

Matches in Nanopublications for { ?s ?p "[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."@en ?g. }

• 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." provenance.
• 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.
• NP196389.RARPwXiThQuJ71VuC1BCvvR4INmTzuUz9zU5GceWfZL3E130_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." NP196389.RARPwXiThQuJ71VuC1BCvvR4INmTzuUz9zU5GceWfZL3E130_provenance.
• 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.
• 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.
• NP873863.RAbCrZMMi8F-yqKQvA9h_GFcPHkhJqydLIwGBmCkDbeJQ130_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." NP873863.RAbCrZMMi8F-yqKQvA9h_GFcPHkhJqydLIwGBmCkDbeJQ130_provenance.
• NP461554.RAD9czdd6kceTSRyd1VlYXD80fKXzk9aecltx3buHsh4k130_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." NP461554.RAD9czdd6kceTSRyd1VlYXD80fKXzk9aecltx3buHsh4k130_provenance.
• 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.
• NP461550.RAkjYieXsuo8mylBVIHuYhNQb_mh7RKLnGCG5FWFOm-Tg130_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." NP461550.RAkjYieXsuo8mylBVIHuYhNQb_mh7RKLnGCG5FWFOm-Tg130_provenance.
• NP461553.RAr3aFlcjQlgtPa798kUnwIMe-36J7eK99MyTVBA-b8H8130_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." NP461553.RAr3aFlcjQlgtPa798kUnwIMe-36J7eK99MyTVBA-b8H8130_provenance.
• NP228581.RA-2pGYlPIMYwLGo8T1huDVCUr0BZsfmMiAjUj8AAwGsk130_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." NP228581.RA-2pGYlPIMYwLGo8T1huDVCUr0BZsfmMiAjUj8AAwGsk130_provenance.
• NP873842.RAzWmCFURdMdnDgcAmWY-9uJcp3CdTJBV3eNEfTHcmuAY130_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." NP873842.RAzWmCFURdMdnDgcAmWY-9uJcp3CdTJBV3eNEfTHcmuAY130_provenance.