Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP183850.RAOU1hvWTJwSyWhqP9hNe39jF29yrU222hl9cKDqwPLRI130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP183850.RAOU1hvWTJwSyWhqP9hNe39jF29yrU222hl9cKDqwPLRI130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP183850.RAOU1hvWTJwSyWhqP9hNe39jF29yrU222hl9cKDqwPLRI130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP183850.RAOU1hvWTJwSyWhqP9hNe39jF29yrU222hl9cKDqwPLRI130_provenance.
- NP183850.RAOU1hvWTJwSyWhqP9hNe39jF29yrU222hl9cKDqwPLRI130_assertion description "[At the screening stage, we examined associations between 63 common single-nucleotide polymorphisms (SNPs) in five genes of this pathway (FGF21, KLB, FGFR1, FGFR2, FGFR3) and four metabolic phenotypes (LDL cholesterol - LDL-C, HDL-cholesterol - HDL-C, triglycerides and body mass index) in 629 individuals from Silesian Hypertension Study (SHS).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP183850.RAOU1hvWTJwSyWhqP9hNe39jF29yrU222hl9cKDqwPLRI130_provenance.
- NP183850.RAOU1hvWTJwSyWhqP9hNe39jF29yrU222hl9cKDqwPLRI130_assertion evidence source_evidence_literature NP183850.RAOU1hvWTJwSyWhqP9hNe39jF29yrU222hl9cKDqwPLRI130_provenance.
- NP183850.RAOU1hvWTJwSyWhqP9hNe39jF29yrU222hl9cKDqwPLRI130_assertion SIO_000772 20717167 NP183850.RAOU1hvWTJwSyWhqP9hNe39jF29yrU222hl9cKDqwPLRI130_provenance.
- NP183850.RAOU1hvWTJwSyWhqP9hNe39jF29yrU222hl9cKDqwPLRI130_assertion wasDerivedFrom gad-20150221 NP183850.RAOU1hvWTJwSyWhqP9hNe39jF29yrU222hl9cKDqwPLRI130_provenance.
- NP183850.RAOU1hvWTJwSyWhqP9hNe39jF29yrU222hl9cKDqwPLRI130_assertion wasGeneratedBy ECO_0000203 NP183850.RAOU1hvWTJwSyWhqP9hNe39jF29yrU222hl9cKDqwPLRI130_provenance.
- gad-20150221 importedOn "2015-02-21" NP183850.RAOU1hvWTJwSyWhqP9hNe39jF29yrU222hl9cKDqwPLRI130_provenance.