Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP676735.RAU0QbHLY-39KLB_siN55gLjQLaLjGoz7BXoc3kPKXQ6U130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP676735.RAU0QbHLY-39KLB_siN55gLjQLaLjGoz7BXoc3kPKXQ6U130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP676735.RAU0QbHLY-39KLB_siN55gLjQLaLjGoz7BXoc3kPKXQ6U130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP676735.RAU0QbHLY-39KLB_siN55gLjQLaLjGoz7BXoc3kPKXQ6U130_provenance.
- 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.
- befree-20150227 importedOn "2015-02-27" NP676735.RAU0QbHLY-39KLB_siN55gLjQLaLjGoz7BXoc3kPKXQ6U130_provenance.