Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP317609.RArjJiT7L218OoPMigN234kn5t-ZRvgS69QLuPU8XXXbI130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP317609.RArjJiT7L218OoPMigN234kn5t-ZRvgS69QLuPU8XXXbI130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP317609.RArjJiT7L218OoPMigN234kn5t-ZRvgS69QLuPU8XXXbI130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP317609.RArjJiT7L218OoPMigN234kn5t-ZRvgS69QLuPU8XXXbI130_provenance.
- NP317609.RArjJiT7L218OoPMigN234kn5t-ZRvgS69QLuPU8XXXbI130_assertion description "[After adjustment for multiple testing, we found a strong association between CLL risk and six genetic variants: CCNH (rs2266690, V270A), APAF1 (rs17028658, 3'region), IL16 (rs4505265, first intron), CASP8 (rs1045485, D302H), NOS2A (rs2779251, promoter), and CCR7 (rs3136687, intron 1).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP317609.RArjJiT7L218OoPMigN234kn5t-ZRvgS69QLuPU8XXXbI130_provenance.
- NP317609.RArjJiT7L218OoPMigN234kn5t-ZRvgS69QLuPU8XXXbI130_assertion evidence source_evidence_literature NP317609.RArjJiT7L218OoPMigN234kn5t-ZRvgS69QLuPU8XXXbI130_provenance.
- NP317609.RArjJiT7L218OoPMigN234kn5t-ZRvgS69QLuPU8XXXbI130_assertion SIO_000772 19074885 NP317609.RArjJiT7L218OoPMigN234kn5t-ZRvgS69QLuPU8XXXbI130_provenance.
- NP317609.RArjJiT7L218OoPMigN234kn5t-ZRvgS69QLuPU8XXXbI130_assertion wasDerivedFrom befree-20150227 NP317609.RArjJiT7L218OoPMigN234kn5t-ZRvgS69QLuPU8XXXbI130_provenance.
- NP317609.RArjJiT7L218OoPMigN234kn5t-ZRvgS69QLuPU8XXXbI130_assertion wasGeneratedBy ECO_0000203 NP317609.RArjJiT7L218OoPMigN234kn5t-ZRvgS69QLuPU8XXXbI130_provenance.
- befree-20150227 importedOn "2015-02-27" NP317609.RArjJiT7L218OoPMigN234kn5t-ZRvgS69QLuPU8XXXbI130_provenance.