Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP196389.RARPwXiThQuJ71VuC1BCvvR4INmTzuUz9zU5GceWfZL3E130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP196389.RARPwXiThQuJ71VuC1BCvvR4INmTzuUz9zU5GceWfZL3E130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP196389.RARPwXiThQuJ71VuC1BCvvR4INmTzuUz9zU5GceWfZL3E130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP196389.RARPwXiThQuJ71VuC1BCvvR4INmTzuUz9zU5GceWfZL3E130_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.
- NP196389.RARPwXiThQuJ71VuC1BCvvR4INmTzuUz9zU5GceWfZL3E130_assertion evidence source_evidence_literature NP196389.RARPwXiThQuJ71VuC1BCvvR4INmTzuUz9zU5GceWfZL3E130_provenance.
- NP196389.RARPwXiThQuJ71VuC1BCvvR4INmTzuUz9zU5GceWfZL3E130_assertion SIO_000772 15389319 NP196389.RARPwXiThQuJ71VuC1BCvvR4INmTzuUz9zU5GceWfZL3E130_provenance.
- NP196389.RARPwXiThQuJ71VuC1BCvvR4INmTzuUz9zU5GceWfZL3E130_assertion wasDerivedFrom befree-20140225 NP196389.RARPwXiThQuJ71VuC1BCvvR4INmTzuUz9zU5GceWfZL3E130_provenance.
- NP196389.RARPwXiThQuJ71VuC1BCvvR4INmTzuUz9zU5GceWfZL3E130_assertion wasGeneratedBy ECO_0000203 NP196389.RARPwXiThQuJ71VuC1BCvvR4INmTzuUz9zU5GceWfZL3E130_provenance.
- befree-20140225 importedOn "2014-02-25" NP196389.RARPwXiThQuJ71VuC1BCvvR4INmTzuUz9zU5GceWfZL3E130_provenance.