Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP29263.RA5fR20DyQbz8oTzgwc7-Ddc1sq7qj4GQ621u36bNV6yA130_assertion> ?p ?o ?g. }
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- NP29263.RA5fR20DyQbz8oTzgwc7-Ddc1sq7qj4GQ621u36bNV6yA130_assertion type Assertion NP29263.RA5fR20DyQbz8oTzgwc7-Ddc1sq7qj4GQ621u36bNV6yA130_head.
- NP29263.RA5fR20DyQbz8oTzgwc7-Ddc1sq7qj4GQ621u36bNV6yA130_assertion description "[Z alpha-1 antitrypsin (AAT) deficiency is a genetic disease associated with accumulation of misfolded AAT in the endoplasmic reticulum (ER) of hepatocytes.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP29263.RA5fR20DyQbz8oTzgwc7-Ddc1sq7qj4GQ621u36bNV6yA130_provenance.
- NP29263.RA5fR20DyQbz8oTzgwc7-Ddc1sq7qj4GQ621u36bNV6yA130_assertion evidence source_evidence_curated NP29263.RA5fR20DyQbz8oTzgwc7-Ddc1sq7qj4GQ621u36bNV6yA130_provenance.
- NP29263.RA5fR20DyQbz8oTzgwc7-Ddc1sq7qj4GQ621u36bNV6yA130_assertion SIO_000772 17559149 NP29263.RA5fR20DyQbz8oTzgwc7-Ddc1sq7qj4GQ621u36bNV6yA130_provenance.
- NP29263.RA5fR20DyQbz8oTzgwc7-Ddc1sq7qj4GQ621u36bNV6yA130_assertion wasDerivedFrom ctd_human-20130708 NP29263.RA5fR20DyQbz8oTzgwc7-Ddc1sq7qj4GQ621u36bNV6yA130_provenance.
- NP29263.RA5fR20DyQbz8oTzgwc7-Ddc1sq7qj4GQ621u36bNV6yA130_assertion wasGeneratedBy ECO_0000218 NP29263.RA5fR20DyQbz8oTzgwc7-Ddc1sq7qj4GQ621u36bNV6yA130_provenance.