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DESCRIBE <http://purl.uniprot.org/SHA-384/B7589ACECD93A9AB9D27AEEF5804F323F37DEC49D620067EB1BBCE4EE79C74D1EB7055F98A41C0563249749360F6FA77>
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http://purl.uniprot.org/SHA-384/B7589ACECD93A9AB9D27AEEF5804F323F37DEC49D620067EB1BBCE4EE79C74D1EB7055F98A41C0563249749360F6FA77
http://www.w3.org/1999/02/22-rdf-syntax-ns#type
http://purl.uniprot.org/core/Annotation
http://purl.uniprot.org/SHA-384/B7589ACECD93A9AB9D27AEEF5804F323F37DEC49D620067EB1BBCE4EE79C74D1EB7055F98A41C0563249749360F6FA77
http://www.w3.org/2000/01/rdf-schema#comment
"Observational study of gene-disease association. (HuGE Navigator); Loss of heterozygosity at NOD2 was observed in only 1 of the 33 colorectal cancer samples. Results suggest that NOD2 3020insC alone does not contribute to CRC risk."
xsd:string
http://purl.uniprot.org/uniprot/#_A24AC707071B065538AB7B404B33C287F714BC2B1EAB08D1D1962BFEF5EF28D3ABA07D1DE0271C9F832A063314F53CAE
http://www.w3.org/1999/02/22-rdf-syntax-ns#subject
http://purl.uniprot.org/SHA-384/B7589ACECD93A9AB9D27AEEF5804F323F37DEC49D620067EB1BBCE4EE79C74D1EB7055F98A41C0563249749360F6FA77
http://purl.uniprot.org/uniprot/D9N2T7
http://purl.uniprot.org/core/mappedAnnotation
http://purl.uniprot.org/SHA-384/B7589ACECD93A9AB9D27AEEF5804F323F37DEC49D620067EB1BBCE4EE79C74D1EB7055F98A41C0563249749360F6FA77
http://purl.uniprot.org/uniprot/#_D9N2T7-mappedCitation-15492242
http://purl.uniprot.org/core/mappedAnnotation
http://purl.uniprot.org/SHA-384/B7589ACECD93A9AB9D27AEEF5804F323F37DEC49D620067EB1BBCE4EE79C74D1EB7055F98A41C0563249749360F6FA77