Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP676735.RAU0QbHLY-39KLB_siN55gLjQLaLjGoz7BXoc3kPKXQ6U130_assertion> ?p ?o ?g. }
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- NP676735.RAU0QbHLY-39KLB_siN55gLjQLaLjGoz7BXoc3kPKXQ6U130_assertion type Assertion NP676735.RAU0QbHLY-39KLB_siN55gLjQLaLjGoz7BXoc3kPKXQ6U130_head.
- NP676735.RAU0QbHLY-39KLB_siN55gLjQLaLjGoz7BXoc3kPKXQ6U130_assertion description "[Across RXRA, one haplotype located 3' of the coding sequence (rs748964, rs3118523), increased RCC risk 35% among individuals with the variant haplotype compared to those with the most common haplotype.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP676735.RAU0QbHLY-39KLB_siN55gLjQLaLjGoz7BXoc3kPKXQ6U130_provenance.
- NP676735.RAU0QbHLY-39KLB_siN55gLjQLaLjGoz7BXoc3kPKXQ6U130_assertion evidence source_evidence_literature NP676735.RAU0QbHLY-39KLB_siN55gLjQLaLjGoz7BXoc3kPKXQ6U130_provenance.
- NP676735.RAU0QbHLY-39KLB_siN55gLjQLaLjGoz7BXoc3kPKXQ6U130_assertion SIO_000772 19753122 NP676735.RAU0QbHLY-39KLB_siN55gLjQLaLjGoz7BXoc3kPKXQ6U130_provenance.
- NP676735.RAU0QbHLY-39KLB_siN55gLjQLaLjGoz7BXoc3kPKXQ6U130_assertion wasDerivedFrom befree-20150227 NP676735.RAU0QbHLY-39KLB_siN55gLjQLaLjGoz7BXoc3kPKXQ6U130_provenance.
- NP676735.RAU0QbHLY-39KLB_siN55gLjQLaLjGoz7BXoc3kPKXQ6U130_assertion wasGeneratedBy ECO_0000203 NP676735.RAU0QbHLY-39KLB_siN55gLjQLaLjGoz7BXoc3kPKXQ6U130_provenance.