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- source_evidence_literature type ECO_0000212 NP1293303.RAp3CuFw0WjaQHhmQgGyo-HfvoMZeReGSNmkGVYDIYO7w130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP1293303.RAp3CuFw0WjaQHhmQgGyo-HfvoMZeReGSNmkGVYDIYO7w130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP1293303.RAp3CuFw0WjaQHhmQgGyo-HfvoMZeReGSNmkGVYDIYO7w130_provenance.
- NP1293303.RAp3CuFw0WjaQHhmQgGyo-HfvoMZeReGSNmkGVYDIYO7w130_assertion description "[We analyzed whether HMOX1 and HMOX2 genes are related with the risk to develop RLS.We analyzed the distribution of genotypes and allelic frequencies of the HMOX1 rs2071746, HMOX1 rs2071747, HMOX2 rs2270363, and HMOX2 rs1051308 SNPs, as well as the presence of Copy number variations (CNVs) of these genes in 205 subjects RLS and 445 healthy controls.The frequencies of rs2071746TT genotype and rs2071746T allelic variant were significantly lower in RLS patients than that in controls, although the other 3 studied SNPs did not differ between RLS patients and controls.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1293303.RAp3CuFw0WjaQHhmQgGyo-HfvoMZeReGSNmkGVYDIYO7w130_provenance.
- NP1293303.RAp3CuFw0WjaQHhmQgGyo-HfvoMZeReGSNmkGVYDIYO7w130_assertion evidence source_evidence_literature NP1293303.RAp3CuFw0WjaQHhmQgGyo-HfvoMZeReGSNmkGVYDIYO7w130_provenance.
- NP1293303.RAp3CuFw0WjaQHhmQgGyo-HfvoMZeReGSNmkGVYDIYO7w130_assertion SIO_000772 26313808 NP1293303.RAp3CuFw0WjaQHhmQgGyo-HfvoMZeReGSNmkGVYDIYO7w130_provenance.
- NP1293303.RAp3CuFw0WjaQHhmQgGyo-HfvoMZeReGSNmkGVYDIYO7w130_assertion wasDerivedFrom befree-2016 NP1293303.RAp3CuFw0WjaQHhmQgGyo-HfvoMZeReGSNmkGVYDIYO7w130_provenance.
- NP1293303.RAp3CuFw0WjaQHhmQgGyo-HfvoMZeReGSNmkGVYDIYO7w130_assertion wasGeneratedBy ECO_0000203 NP1293303.RAp3CuFw0WjaQHhmQgGyo-HfvoMZeReGSNmkGVYDIYO7w130_provenance.
- befree-2016 importedOn "2016-02-19" NP1293303.RAp3CuFw0WjaQHhmQgGyo-HfvoMZeReGSNmkGVYDIYO7w130_provenance.