Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP87041.RAeBRNOhJO1Tk9Cqk-kgXDtvWntdwj_Hh75i-WTGUmvVE130_assertion> ?p ?o ?g. }
Showing items 1 to 6 of
6
with 100 items per page.
- NP87041.RAeBRNOhJO1Tk9Cqk-kgXDtvWntdwj_Hh75i-WTGUmvVE130_assertion type Assertion NP87041.RAeBRNOhJO1Tk9Cqk-kgXDtvWntdwj_Hh75i-WTGUmvVE130_head.
- NP87041.RAeBRNOhJO1Tk9Cqk-kgXDtvWntdwj_Hh75i-WTGUmvVE130_assertion description "[Analyzing the C599T (Pro200Leu) polymorphism in the GPX1 gene PTDM was diagnosed in 8.45% of patients with CC genotype, 13.43% with CT and in 28.57% with TT.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP87041.RAeBRNOhJO1Tk9Cqk-kgXDtvWntdwj_Hh75i-WTGUmvVE130_provenance.
- NP87041.RAeBRNOhJO1Tk9Cqk-kgXDtvWntdwj_Hh75i-WTGUmvVE130_assertion evidence source_evidence_literature NP87041.RAeBRNOhJO1Tk9Cqk-kgXDtvWntdwj_Hh75i-WTGUmvVE130_provenance.
- NP87041.RAeBRNOhJO1Tk9Cqk-kgXDtvWntdwj_Hh75i-WTGUmvVE130_assertion SIO_000772 20851292 NP87041.RAeBRNOhJO1Tk9Cqk-kgXDtvWntdwj_Hh75i-WTGUmvVE130_provenance.
- NP87041.RAeBRNOhJO1Tk9Cqk-kgXDtvWntdwj_Hh75i-WTGUmvVE130_assertion wasDerivedFrom gad-20130706 NP87041.RAeBRNOhJO1Tk9Cqk-kgXDtvWntdwj_Hh75i-WTGUmvVE130_provenance.
- NP87041.RAeBRNOhJO1Tk9Cqk-kgXDtvWntdwj_Hh75i-WTGUmvVE130_assertion wasGeneratedBy ECO_0000203 NP87041.RAeBRNOhJO1Tk9Cqk-kgXDtvWntdwj_Hh75i-WTGUmvVE130_provenance.