Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP87041.RAeBRNOhJO1Tk9Cqk-kgXDtvWntdwj_Hh75i-WTGUmvVE130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP87041.RAeBRNOhJO1Tk9Cqk-kgXDtvWntdwj_Hh75i-WTGUmvVE130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP87041.RAeBRNOhJO1Tk9Cqk-kgXDtvWntdwj_Hh75i-WTGUmvVE130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP87041.RAeBRNOhJO1Tk9Cqk-kgXDtvWntdwj_Hh75i-WTGUmvVE130_provenance.
- 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.
- gad-20130706 importedOn "2013-07-06" NP87041.RAeBRNOhJO1Tk9Cqk-kgXDtvWntdwj_Hh75i-WTGUmvVE130_provenance.