Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP718849.RABIhpnDseLuaVzLichdcP2Va02TyasLJpl5hHdRJkivo130_assertion> ?p ?o ?g. }
Showing items 1 to 6 of
6
with 100 items per page.
- NP718849.RABIhpnDseLuaVzLichdcP2Va02TyasLJpl5hHdRJkivo130_assertion type Assertion NP718849.RABIhpnDseLuaVzLichdcP2Va02TyasLJpl5hHdRJkivo130_head.
- NP718849.RABIhpnDseLuaVzLichdcP2Va02TyasLJpl5hHdRJkivo130_assertion wasGeneratedBy ECO_0000203 NP718849.RABIhpnDseLuaVzLichdcP2Va02TyasLJpl5hHdRJkivo130_provenance.
- NP718849.RABIhpnDseLuaVzLichdcP2Va02TyasLJpl5hHdRJkivo130_assertion wasDerivedFrom befree-2016 NP718849.RABIhpnDseLuaVzLichdcP2Va02TyasLJpl5hHdRJkivo130_provenance.
- NP718849.RABIhpnDseLuaVzLichdcP2Va02TyasLJpl5hHdRJkivo130_assertion SIO_000772 19195941 NP718849.RABIhpnDseLuaVzLichdcP2Va02TyasLJpl5hHdRJkivo130_provenance.
- NP718849.RABIhpnDseLuaVzLichdcP2Va02TyasLJpl5hHdRJkivo130_assertion evidence source_evidence_literature NP718849.RABIhpnDseLuaVzLichdcP2Va02TyasLJpl5hHdRJkivo130_provenance.
- NP718849.RABIhpnDseLuaVzLichdcP2Va02TyasLJpl5hHdRJkivo130_assertion description "[Our data further expand the spectrum of POLG1 gene mutations and the unique phenotype reported (late onset isolated liver disease without lactic acidosis) increase the variability of clinical presentations associated with mutations in this gene.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP718849.RABIhpnDseLuaVzLichdcP2Va02TyasLJpl5hHdRJkivo130_provenance.