Matches in Nanopublications for { ?s ?p "[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."@en ?g. }
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- NP125792.RASd8mU986JYwn0FjffHndMxYnygsjGwJQljecbulMUbU130_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." NP125792.RASd8mU986JYwn0FjffHndMxYnygsjGwJQljecbulMUbU130_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.
- 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." provenance.
- 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." provenance.
- NP156417.RAFu_BiL8RQc-E7rDPG4Beh9W1gDqShvi9daxyQ0IxkWg130_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." NP156417.RAFu_BiL8RQc-E7rDPG4Beh9W1gDqShvi9daxyQ0IxkWg130_provenance.
- NP763125.RA0ODBaGP_GY8xFOgByPltdNd3fnmklxY7MKg9wrdvMg4130_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." NP763125.RA0ODBaGP_GY8xFOgByPltdNd3fnmklxY7MKg9wrdvMg4130_provenance.