Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP184299.RAF_7zlz41cAabHdgPVlqeY0AcSSLtVUkkRn3ClxGbNBg130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP184299.RAF_7zlz41cAabHdgPVlqeY0AcSSLtVUkkRn3ClxGbNBg130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP184299.RAF_7zlz41cAabHdgPVlqeY0AcSSLtVUkkRn3ClxGbNBg130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP184299.RAF_7zlz41cAabHdgPVlqeY0AcSSLtVUkkRn3ClxGbNBg130_provenance.
- NP184299.RAF_7zlz41cAabHdgPVlqeY0AcSSLtVUkkRn3ClxGbNBg130_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." NP184299.RAF_7zlz41cAabHdgPVlqeY0AcSSLtVUkkRn3ClxGbNBg130_provenance.
- NP184299.RAF_7zlz41cAabHdgPVlqeY0AcSSLtVUkkRn3ClxGbNBg130_assertion evidence source_evidence_literature NP184299.RAF_7zlz41cAabHdgPVlqeY0AcSSLtVUkkRn3ClxGbNBg130_provenance.
- NP184299.RAF_7zlz41cAabHdgPVlqeY0AcSSLtVUkkRn3ClxGbNBg130_assertion SIO_000772 20717167 NP184299.RAF_7zlz41cAabHdgPVlqeY0AcSSLtVUkkRn3ClxGbNBg130_provenance.
- NP184299.RAF_7zlz41cAabHdgPVlqeY0AcSSLtVUkkRn3ClxGbNBg130_assertion wasDerivedFrom befree-20140225 NP184299.RAF_7zlz41cAabHdgPVlqeY0AcSSLtVUkkRn3ClxGbNBg130_provenance.
- NP184299.RAF_7zlz41cAabHdgPVlqeY0AcSSLtVUkkRn3ClxGbNBg130_assertion wasGeneratedBy ECO_0000203 NP184299.RAF_7zlz41cAabHdgPVlqeY0AcSSLtVUkkRn3ClxGbNBg130_provenance.
- befree-20140225 importedOn "2014-02-25" NP184299.RAF_7zlz41cAabHdgPVlqeY0AcSSLtVUkkRn3ClxGbNBg130_provenance.