{"meta":{"query_hash":"48e6fea7a641","filters":{"venue":"Gene Function & Disease"},"cohort_total":3,"direct_labels_cover":0,"predictions_cover":3,"exported":3,"export_cap":100000,"truncated":false,"label_status":"direct model label, unvalidated","prediction_status":"machine_predicted_unvalidated (Codex and Gemma teacher distillation)","score_status":"score_only:v0-immature-baseline","snapshot":{"source":"OpenAlex, pinned release, all 482 partitions","release":"2026-06-24","frame_built":"2026-07-12"},"permalink":"https://metacan.xera.ac/q/48e6fea7a641","api":"https://metacan.xera.ac/api/v1/cohort?venue=Gene+Function+%26+Disease"},"results":[{"id":"W1971133648","doi":"10.1002/1438-826x(200010)1:3/4<134::aid-gnfd134>3.0.co;2-w","title":"Skeletal myopathy in mice over-expressing the human myotonic dystrophy protein kinase (DMPK) gene","year":2000,"lang":"en","type":"article","venue":"Gene Function & Disease","topic":"Genetic Neurodegenerative Diseases","field":"Neuroscience","cited_by":2,"is_retracted":false,"has_abstract":true,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"BC Children's Hospital; University of Ottawa; University of British Columbia; Children's Hospital of Eastern Ontario","funders":"","keywords":"Myotonic dystrophy; Myogenesis; Skeletal muscle; Biology; Myopathy; C2C12; Genetically modified mouse; Muscular dystrophy; Trinucleotide repeat expansion; Myotonia; Myocyte; Transgene; Muscle atrophy; Protein kinase A; Endocrinology; Internal medicine; Gene; Kinase; Cell biology; Genetics; Medicine; Allele","score_opus":0.016754339554653472,"score_gpt":0.24303136416251353,"score_spread":0.22627702460786006,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W1971133648","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.9711761,0.0028603578,0.008679663,0.0009971528,0.00020664193,0.00050135626,0.0060906145,0.0013816197,0.0081066005],"genre_scores_gemma":[0.93100846,0.0047092987,0.017759591,0.0006306451,0.00009694267,0.0011020905,0.007116944,0.00047236696,0.037103627],"study_design_codex":"bench_or_experimental","study_design_gemma":"bench_or_experimental","domain_scores_codex":[0.9994648,0.000088732864,0.00006978014,0.00018297508,0.00010370342,0.0000899993],"domain_scores_gemma":[0.99968326,0.000061514256,0.00010896526,0.000024854244,0.000018052264,0.000103481354],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0005996816,0.0016316187,0.00052053836,0.0017358705,0.0009560475,0.00065972214,0.0005843861,0.0018743791,0.0059915255],"category_scores_gemma":[0.00023369935,0.0010039911,0.0005879034,0.0005563889,0.001096081,0.00067116745,0.000695954,0.001844022,0.002293503],"study_design_candidate":"bench_or_experimental","study_design_consensus":"bench_or_experimental","about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.00047825527,0.00031671167,0.0003663196,0.00009728198,0.000029565894,0.0005433524,0.00011709094,0.00012865812,0.99447,0.0008939949,0.0003004265,0.0022583907],"study_design_scores_gemma":[0.0012852043,0.0038331915,0.018199781,0.0002487199,0.00026863432,0.008002547,0.00025192118,0.0032843698,0.9380862,0.0011826805,0.025293536,0.00006325436],"about_ca_topic_score_codex":0.0012063115,"about_ca_topic_score_gemma":0.0024443946,"teacher_disagreement_score":0.0059915255,"about_ca_system_score_codex":0.00057720946,"about_ca_system_score_gemma":0.0004921549,"threshold_uncertainty_score":0.020043612},"labels":[],"label_agreement":null},{"id":"W2058488105","doi":"10.1002/1438-826x(200012)1:5/6<194::aid-gnfd194>3.0.co;2-2","title":"Identification of polymorphisms in the GABAB receptor gene and linkage study of attention-deficit hyperactivity disorder","year":2000,"lang":"en","type":"article","venue":"Gene Function & Disease","topic":"Attention Deficit Hyperactivity Disorder","field":"Medicine","cited_by":4,"is_retracted":false,"has_abstract":true,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"Centre for Addiction and Mental Health; University Health Network; University of Toronto; SickKids Foundation; Hospital for Sick Children; Toronto Western Hospital","funders":"","keywords":"Genetics; Genetic linkage; Candidate gene; Proband; Biology; Attention deficit hyperactivity disorder; Gene; Psychology; Mutation; Psychiatry","score_opus":0.01954032466410499,"score_gpt":0.27511372941329204,"score_spread":0.25557340474918705,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2058488105","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.99772066,0.0007056721,0.00030297076,0.00017960236,0.000018854278,0.000023809982,0.00020415666,0.00000767621,0.00083653274],"genre_scores_gemma":[0.99794406,0.0005572367,0.0005960777,0.00008848336,0.00003626031,0.000034990993,0.00023885883,0.0000054106563,0.0004986727],"study_design_codex":"observational","study_design_gemma":"observational","domain_scores_codex":[0.9991217,0.00032048204,0.000078081204,0.00021617957,0.00018563864,0.00007774253],"domain_scores_gemma":[0.9990901,0.00038420904,0.00022434462,0.00005710439,0.00009190241,0.00015224628],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00070325227,0.0006549319,0.00047054558,0.0017724067,0.0011872754,0.0005041449,0.00046648266,0.00075817277,0.002892843],"category_scores_gemma":[0.003941002,0.00041495587,0.00025072618,0.0013775534,0.0004399291,0.00023435647,0.0005998079,0.0006873581,0.00028461235],"study_design_candidate":"observational","study_design_consensus":"observational","about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.00083791214,0.0005347819,0.97116697,0.00006702421,0.00044390996,0.0056719715,0.0008818182,0.00013420454,0.007833982,0.000470952,0.00080463197,0.0111518735],"study_design_scores_gemma":[0.00011769308,0.0003781503,0.98414326,0.00004549531,0.0002635907,0.012068862,0.0003298751,0.00042013914,0.000793699,0.00022894911,0.0011980812,0.000012221576],"about_ca_topic_score_codex":0.005155577,"about_ca_topic_score_gemma":0.003949794,"teacher_disagreement_score":0.005155577,"about_ca_system_score_codex":0.0002755225,"about_ca_system_score_gemma":0.00035144197,"threshold_uncertainty_score":0.010251105},"labels":[],"label_agreement":null},{"id":"W2079336224","doi":"10.1002/gnfd.200290001","title":"Structural variation in a novel zinc finger protein and investigation of its role in Hirschsprung disease","year":2002,"lang":"en","type":"article","venue":"Gene Function & Disease","topic":"Congenital gastrointestinal and neural anomalies","field":"Medicine","cited_by":3,"is_retracted":false,"has_abstract":true,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"University of Calgary; Queen's University","funders":"","keywords":"Zinc finger; Neural crest; Biology; Gene; Transcription factor; Genetics; Zinc finger transcription factor; Phenotype; TCF4; Transcription (linguistics)","score_opus":0.0224468714168827,"score_gpt":0.2069262659201228,"score_spread":0.1844793945032401,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2079336224","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.99918133,0.00014077053,0.00037459697,0.000024661424,0.000006803554,0.000005803753,0.0001221067,0.000008100328,0.00013574939],"genre_scores_gemma":[0.9993967,0.000038222188,0.0003545409,0.000015282776,0.0000058059836,0.0000023610758,0.000088091096,0.0000026352618,0.000096344935],"study_design_codex":"bench_or_experimental","study_design_gemma":"observational","domain_scores_codex":[0.99983585,0.000024933443,0.000025541256,0.000052534604,0.00003630584,0.000024823472],"domain_scores_gemma":[0.9997787,0.00006139306,0.000070593596,0.000009841296,0.000019298497,0.000060234095],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0001709823,0.00034870283,0.00022023417,0.0009547731,0.00026829808,0.00017813894,0.00030529973,0.00055801007,0.0009471808],"category_scores_gemma":[0.00036059952,0.0000959634,0.00037076444,0.00048699594,0.0003370884,0.00010576649,0.00022921323,0.0002698136,0.00011084834],"study_design_candidate":"observational","study_design_consensus":null,"about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.0018858896,0.00033208725,0.12927422,0.00015033042,0.00027415913,0.03894541,0.00048119342,0.0008344907,0.81481403,0.0010754142,0.00025986662,0.0116729615],"study_design_scores_gemma":[0.00024318811,0.0023873302,0.79597956,0.000058478076,0.00038030354,0.09111062,0.00035752507,0.0041542337,0.09891992,0.00093765865,0.0054044197,0.00006677177],"about_ca_topic_score_codex":0.001109148,"about_ca_topic_score_gemma":0.0008899253,"teacher_disagreement_score":0.001109148,"about_ca_system_score_codex":0.0001974424,"about_ca_system_score_gemma":0.00012042735,"threshold_uncertainty_score":0.0031686425},"labels":[],"label_agreement":null}]}