Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP449514.RAIA7uGVuBer2yj-vwJjNQDoUcaSS1TBWlyYex0GfZ5HQ130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP449514.RAIA7uGVuBer2yj-vwJjNQDoUcaSS1TBWlyYex0GfZ5HQ130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP449514.RAIA7uGVuBer2yj-vwJjNQDoUcaSS1TBWlyYex0GfZ5HQ130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP449514.RAIA7uGVuBer2yj-vwJjNQDoUcaSS1TBWlyYex0GfZ5HQ130_provenance.
- NP449514.RAIA7uGVuBer2yj-vwJjNQDoUcaSS1TBWlyYex0GfZ5HQ130_assertion description "[To investigate if common variants of CYP1A2, CYP1B1, CYP3A4, CYP3A5, CYP11A1, CYP17A1 and CYP19A1 influence CRC risk we genotyped 2,575 CRC cases and 2,707 controls for 20 single nucleotide polymorphisms (SNPs) that have not previously been shown to have functional consequence within these genes.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP449514.RAIA7uGVuBer2yj-vwJjNQDoUcaSS1TBWlyYex0GfZ5HQ130_provenance.
- NP449514.RAIA7uGVuBer2yj-vwJjNQDoUcaSS1TBWlyYex0GfZ5HQ130_assertion evidence source_evidence_literature NP449514.RAIA7uGVuBer2yj-vwJjNQDoUcaSS1TBWlyYex0GfZ5HQ130_provenance.
- NP449514.RAIA7uGVuBer2yj-vwJjNQDoUcaSS1TBWlyYex0GfZ5HQ130_assertion SIO_000772 17615053 NP449514.RAIA7uGVuBer2yj-vwJjNQDoUcaSS1TBWlyYex0GfZ5HQ130_provenance.
- NP449514.RAIA7uGVuBer2yj-vwJjNQDoUcaSS1TBWlyYex0GfZ5HQ130_assertion wasDerivedFrom befree-20140225 NP449514.RAIA7uGVuBer2yj-vwJjNQDoUcaSS1TBWlyYex0GfZ5HQ130_provenance.
- NP449514.RAIA7uGVuBer2yj-vwJjNQDoUcaSS1TBWlyYex0GfZ5HQ130_assertion wasGeneratedBy ECO_0000203 NP449514.RAIA7uGVuBer2yj-vwJjNQDoUcaSS1TBWlyYex0GfZ5HQ130_provenance.
- befree-20140225 importedOn "2014-02-25" NP449514.RAIA7uGVuBer2yj-vwJjNQDoUcaSS1TBWlyYex0GfZ5HQ130_provenance.