Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP558068.RAnfjeuFdipN8f_oGQf9LPEBxLX9AVn-Un7MhYKc_KA8I130_assertion> ?p ?o ?g. }
Showing items 1 to 6 of
6
with 100 items per page.
- NP558068.RAnfjeuFdipN8f_oGQf9LPEBxLX9AVn-Un7MhYKc_KA8I130_assertion type Assertion NP558068.RAnfjeuFdipN8f_oGQf9LPEBxLX9AVn-Un7MhYKc_KA8I130_head.
- NP558068.RAnfjeuFdipN8f_oGQf9LPEBxLX9AVn-Un7MhYKc_KA8I130_assertion description "[Heritable mutations in the ttpA gene, encoding for TTP, result in ataxia with vitamin E deficiency (AVED) syndrome, typified by low vitamin E levels and a plethora of neurological disorders.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP558068.RAnfjeuFdipN8f_oGQf9LPEBxLX9AVn-Un7MhYKc_KA8I130_provenance.
- NP558068.RAnfjeuFdipN8f_oGQf9LPEBxLX9AVn-Un7MhYKc_KA8I130_assertion evidence source_evidence_literature NP558068.RAnfjeuFdipN8f_oGQf9LPEBxLX9AVn-Un7MhYKc_KA8I130_provenance.
- NP558068.RAnfjeuFdipN8f_oGQf9LPEBxLX9AVn-Un7MhYKc_KA8I130_assertion SIO_000772 16819822 NP558068.RAnfjeuFdipN8f_oGQf9LPEBxLX9AVn-Un7MhYKc_KA8I130_provenance.
- NP558068.RAnfjeuFdipN8f_oGQf9LPEBxLX9AVn-Un7MhYKc_KA8I130_assertion wasDerivedFrom befree-2016 NP558068.RAnfjeuFdipN8f_oGQf9LPEBxLX9AVn-Un7MhYKc_KA8I130_provenance.
- NP558068.RAnfjeuFdipN8f_oGQf9LPEBxLX9AVn-Un7MhYKc_KA8I130_assertion wasGeneratedBy ECO_0000203 NP558068.RAnfjeuFdipN8f_oGQf9LPEBxLX9AVn-Un7MhYKc_KA8I130_provenance.