Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP195905.RAj60tBvDRDDA5zBwKUQFf4gJ2JunEUJ6njGr91SmlCTE130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP195905.RAj60tBvDRDDA5zBwKUQFf4gJ2JunEUJ6njGr91SmlCTE130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP195905.RAj60tBvDRDDA5zBwKUQFf4gJ2JunEUJ6njGr91SmlCTE130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP195905.RAj60tBvDRDDA5zBwKUQFf4gJ2JunEUJ6njGr91SmlCTE130_provenance.
- NP195905.RAj60tBvDRDDA5zBwKUQFf4gJ2JunEUJ6njGr91SmlCTE130_assertion description "[In two independent case-control studies containing 796 HCC cases and 806 cancer-free individuals, we genotyped two putative functional insertion/deletion (indel) polymorphisms [BRM-1321 (rs3832613) and BRM-741 (rs34480940)] within promoter region of BRM in Chinese populations using a PCR-based method.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP195905.RAj60tBvDRDDA5zBwKUQFf4gJ2JunEUJ6njGr91SmlCTE130_provenance.
- NP195905.RAj60tBvDRDDA5zBwKUQFf4gJ2JunEUJ6njGr91SmlCTE130_assertion evidence source_evidence_literature NP195905.RAj60tBvDRDDA5zBwKUQFf4gJ2JunEUJ6njGr91SmlCTE130_provenance.
- NP195905.RAj60tBvDRDDA5zBwKUQFf4gJ2JunEUJ6njGr91SmlCTE130_assertion SIO_000772 23359823 NP195905.RAj60tBvDRDDA5zBwKUQFf4gJ2JunEUJ6njGr91SmlCTE130_provenance.
- NP195905.RAj60tBvDRDDA5zBwKUQFf4gJ2JunEUJ6njGr91SmlCTE130_assertion wasDerivedFrom befree-20140225 NP195905.RAj60tBvDRDDA5zBwKUQFf4gJ2JunEUJ6njGr91SmlCTE130_provenance.
- NP195905.RAj60tBvDRDDA5zBwKUQFf4gJ2JunEUJ6njGr91SmlCTE130_assertion wasGeneratedBy ECO_0000203 NP195905.RAj60tBvDRDDA5zBwKUQFf4gJ2JunEUJ6njGr91SmlCTE130_provenance.
- befree-20140225 importedOn "2014-02-25" NP195905.RAj60tBvDRDDA5zBwKUQFf4gJ2JunEUJ6njGr91SmlCTE130_provenance.