gda sio_type label comment title id voidSubset
http://rdf.disgenet.org/resource/gda/DGN0008ee23b0b3a42067c422d407d83d76
"gene-disease association linked with genetic variation"@en
"epidermal growth factor receptor [ncbigene:1956] - Metastatic malignant neoplasm to brain [umls:C0220650] Association [disgenet:DGN0008ee23b0b3a42067c422d407d83d76]"@en
"Association between the gene [ncbigene:1956] and the disease [umls:C0220650] integrated into DisGeNET. Gene-disease associations are identified by the DisGeNET ID."@en
"epidermal growth factor receptor [ncbigene:1956] - Metastatic malignant neoplasm to brain [umls:C0220650] Association"@en
"disgenet:DGN0008ee23b0b3a42067c422d407d83d76"^^<http://www.w3.org/2001/XMLSchema#string>
http://rdf.disgenet.org/v6.0.0/void/geneDiseaseAssociation
http://rdf.disgenet.org/resource/gda/DGN0019062a8e5976126e1b97f913e05912
"gene-disease association linked with genetic variation"@en
"cone-rod homeobox [ncbigene:1406] - LEBER CONGENITAL AMAUROSIS 7 [umls:C3151192] Association [disgenet:DGN0019062a8e5976126e1b97f913e05912]"@en
"Association between the gene [ncbigene:1406] and the disease [umls:C3151192] integrated into DisGeNET. Gene-disease associations are identified by the DisGeNET ID."@en
"cone-rod homeobox [ncbigene:1406] - LEBER CONGENITAL AMAUROSIS 7 [umls:C3151192] Association"@en
"disgenet:DGN0019062a8e5976126e1b97f913e05912"^^<http://www.w3.org/2001/XMLSchema#string>
http://rdf.disgenet.org/v6.0.0/void/geneDiseaseAssociation
http://rdf.disgenet.org/resource/gda/DGN001c4185f9c1608d01bf5b8559057c21
"gene-disease association linked with genetic variation"@en
"apolipoprotein E [ncbigene:348] - Alzheimer's Disease [umls:C0002395] Association [disgenet:DGN001c4185f9c1608d01bf5b8559057c21]"@en
"Association between the gene [ncbigene:348] and the disease [umls:C0002395] integrated into DisGeNET. Gene-disease associations are identified by the DisGeNET ID."@en
"apolipoprotein E [ncbigene:348] - Alzheimer's Disease [umls:C0002395] Association"@en
"disgenet:DGN001c4185f9c1608d01bf5b8559057c21"^^<http://www.w3.org/2001/XMLSchema#string>
http://rdf.disgenet.org/v6.0.0/void/geneDiseaseAssociation
http://rdf.disgenet.org/resource/gda/DGN0047408de48823df776be88c10aed4ed
"gene-disease association linked with genetic variation"@en
"crystallin gamma D [ncbigene:1421] - Age-related cataract [umls:C0036646] Association [disgenet:DGN0047408de48823df776be88c10aed4ed]"@en
"Association between the gene [ncbigene:1421] and the disease [umls:C0036646] integrated into DisGeNET. Gene-disease associations are identified by the DisGeNET ID."@en
"crystallin gamma D [ncbigene:1421] - Age-related cataract [umls:C0036646] Association"@en
"disgenet:DGN0047408de48823df776be88c10aed4ed"^^<http://www.w3.org/2001/XMLSchema#string>
http://rdf.disgenet.org/v6.0.0/void/geneDiseaseAssociation
http://rdf.disgenet.org/resource/gda/DGN0047435889aabadc92ccae8ae6c05441
"gene-disease association linked with genetic variation"@en
"general transcription factor IIH subunit 1 [ncbigene:2965] - Osteitis Deformans [umls:C0029401] Association [disgenet:DGN0047435889aabadc92ccae8ae6c05441]"@en
"Association between the gene [ncbigene:2965] and the disease [umls:C0029401] integrated into DisGeNET. Gene-disease associations are identified by the DisGeNET ID."@en
"general transcription factor IIH subunit 1 [ncbigene:2965] - Osteitis Deformans [umls:C0029401] Association"@en
"disgenet:DGN0047435889aabadc92ccae8ae6c05441"^^<http://www.w3.org/2001/XMLSchema#string>
http://rdf.disgenet.org/v6.0.0/void/geneDiseaseAssociation
http://rdf.disgenet.org/resource/gda/DGN004cfb66bab59759a7576447d0cc82da
"gene-disease association linked with genetic variation"@en
"collagen type IV alpha 5 chain [ncbigene:1287] - Alport Syndrome, X-Linked [umls:C1567742] Association [disgenet:DGN004cfb66bab59759a7576447d0cc82da]"@en
"Association between the gene [ncbigene:1287] and the disease [umls:C1567742] integrated into DisGeNET. Gene-disease associations are identified by the DisGeNET ID."@en
"collagen type IV alpha 5 chain [ncbigene:1287] - Alport Syndrome, X-Linked [umls:C1567742] Association"@en
"disgenet:DGN004cfb66bab59759a7576447d0cc82da"^^<http://www.w3.org/2001/XMLSchema#string>
http://rdf.disgenet.org/v6.0.0/void/geneDiseaseAssociation
http://rdf.disgenet.org/resource/gda/DGN005746a4774a4db86a79e83e854195f3
"gene-disease association linked with genetic variation"@en
"apolipoprotein E [ncbigene:348] - Liver diseases [umls:C0023895] Association [disgenet:DGN005746a4774a4db86a79e83e854195f3]"@en
"Association between the gene [ncbigene:348] and the disease [umls:C0023895] integrated into DisGeNET. Gene-disease associations are identified by the DisGeNET ID."@en
"apolipoprotein E [ncbigene:348] - Liver diseases [umls:C0023895] Association"@en
"disgenet:DGN005746a4774a4db86a79e83e854195f3"^^<http://www.w3.org/2001/XMLSchema#string>
http://rdf.disgenet.org/v6.0.0/void/geneDiseaseAssociation
http://rdf.disgenet.org/resource/gda/DGN0061006b92e54749c2597fa07c40fe10
"gene-disease association linked with genetic variation"@en
"ATPase Na+/K+ transporting subunit alpha 3 [ncbigene:478] - Neonatal infection [umls:C0854706] Association [disgenet:DGN0061006b92e54749c2597fa07c40fe10]"@en
"Association between the gene [ncbigene:478] and the disease [umls:C0854706] integrated into DisGeNET. Gene-disease associations are identified by the DisGeNET ID."@en
"ATPase Na+/K+ transporting subunit alpha 3 [ncbigene:478] - Neonatal infection [umls:C0854706] Association"@en
"disgenet:DGN0061006b92e54749c2597fa07c40fe10"^^<http://www.w3.org/2001/XMLSchema#string>
http://rdf.disgenet.org/v6.0.0/void/geneDiseaseAssociation
http://rdf.disgenet.org/resource/gda/DGN00674baa36ec4484bd014f372b466076
"gene-disease association linked with genetic variation"@en
"interleukin 1 receptor antagonist [ncbigene:3557] - X-Linked Lymphoproliferative Disorder [umls:C0549463] Association [disgenet:DGN00674baa36ec4484bd014f372b466076]"@en
"Association between the gene [ncbigene:3557] and the disease [umls:C0549463] integrated into DisGeNET. Gene-disease associations are identified by the DisGeNET ID."@en
"interleukin 1 receptor antagonist [ncbigene:3557] - X-Linked Lymphoproliferative Disorder [umls:C0549463] Association"@en
"disgenet:DGN00674baa36ec4484bd014f372b466076"^^<http://www.w3.org/2001/XMLSchema#string>
http://rdf.disgenet.org/v6.0.0/void/geneDiseaseAssociation
http://rdf.disgenet.org/resource/gda/DGN006ea501218431952fef5f05c2184030
"gene-disease association linked with genetic variation"@en
"epidermal growth factor receptor [ncbigene:1956] - Glioma [umls:C0017638] Association [disgenet:DGN006ea501218431952fef5f05c2184030]"@en
"Association between the gene [ncbigene:1956] and the disease [umls:C0017638] integrated into DisGeNET. Gene-disease associations are identified by the DisGeNET ID."@en
"epidermal growth factor receptor [ncbigene:1956] - Glioma [umls:C0017638] Association"@en
"disgenet:DGN006ea501218431952fef5f05c2184030"^^<http://www.w3.org/2001/XMLSchema#string>
http://rdf.disgenet.org/v6.0.0/void/geneDiseaseAssociation
http://rdf.disgenet.org/resource/gda/DGN00700b00857e14abf2c4c5d4483c3631
"gene-disease association linked with genetic variation"@en
"TNF receptor superfamily member 1B [ncbigene:7133] - Paranoid Schizophrenia [umls:C0036349] Association [disgenet:DGN00700b00857e14abf2c4c5d4483c3631]"@en
"Association between the gene [ncbigene:7133] and the disease [umls:C0036349] integrated into DisGeNET. Gene-disease associations are identified by the DisGeNET ID."@en
"TNF receptor superfamily member 1B [ncbigene:7133] - Paranoid Schizophrenia [umls:C0036349] Association"@en
"disgenet:DGN00700b00857e14abf2c4c5d4483c3631"^^<http://www.w3.org/2001/XMLSchema#string>
http://rdf.disgenet.org/v6.0.0/void/geneDiseaseAssociation
http://rdf.disgenet.org/resource/gda/DGN007f77a85e575be5955dfaf5200f0524
"gene-disease association linked with genetic variation"@en
"NPC intracellular cholesterol transporter 2 [ncbigene:10577] - Progressive supranuclear palsy [umls:C0038868] Association [disgenet:DGN007f77a85e575be5955dfaf5200f0524]"@en
"Association between the gene [ncbigene:10577] and the disease [umls:C0038868] integrated into DisGeNET. Gene-disease associations are identified by the DisGeNET ID."@en
"NPC intracellular cholesterol transporter 2 [ncbigene:10577] - Progressive supranuclear palsy [umls:C0038868] Association"@en
"disgenet:DGN007f77a85e575be5955dfaf5200f0524"^^<http://www.w3.org/2001/XMLSchema#string>
http://rdf.disgenet.org/v6.0.0/void/geneDiseaseAssociation
http://rdf.disgenet.org/resource/gda/DGN009543a7d4782cfe9d8b5bf282189409
"gene-disease association linked with genetic variation"@en
"complement C3 [ncbigene:718] - Arteriosclerosis [umls:C0003850] Association [disgenet:DGN009543a7d4782cfe9d8b5bf282189409]"@en
"Association between the gene [ncbigene:718] and the disease [umls:C0003850] integrated into DisGeNET. Gene-disease associations are identified by the DisGeNET ID."@en
"complement C3 [ncbigene:718] - Arteriosclerosis [umls:C0003850] Association"@en
"disgenet:DGN009543a7d4782cfe9d8b5bf282189409"^^<http://www.w3.org/2001/XMLSchema#string>
http://rdf.disgenet.org/v6.0.0/void/geneDiseaseAssociation
http://rdf.disgenet.org/resource/gda/DGN00981741058f5dc323d6f6890096a3a3
"gene-disease association linked with genetic variation"@en
"steroid 5 alpha-reductase 2 [ncbigene:6716] - Metastasis from malignant tumor of prostate [umls:C1282496] Association [disgenet:DGN00981741058f5dc323d6f6890096a3a3]"@en
"Association between the gene [ncbigene:6716] and the disease [umls:C1282496] integrated into DisGeNET. Gene-disease associations are identified by the DisGeNET ID."@en
"steroid 5 alpha-reductase 2 [ncbigene:6716] - Metastasis from malignant tumor of prostate [umls:C1282496] Association"@en
"disgenet:DGN00981741058f5dc323d6f6890096a3a3"^^<http://www.w3.org/2001/XMLSchema#string>
http://rdf.disgenet.org/v6.0.0/void/geneDiseaseAssociation
http://rdf.disgenet.org/resource/gda/DGN00a287e88f820987f3c8cab684d15122
"gene-disease association linked with genetic variation"@en
"laminin subunit alpha 2 [ncbigene:3908] - Respiratory Failure [umls:C1145670] Association [disgenet:DGN00a287e88f820987f3c8cab684d15122]"@en
"Association between the gene [ncbigene:3908] and the disease [umls:C1145670] integrated into DisGeNET. Gene-disease associations are identified by the DisGeNET ID."@en
"laminin subunit alpha 2 [ncbigene:3908] - Respiratory Failure [umls:C1145670] Association"@en
"disgenet:DGN00a287e88f820987f3c8cab684d15122"^^<http://www.w3.org/2001/XMLSchema#string>
http://rdf.disgenet.org/v6.0.0/void/geneDiseaseAssociation
http://rdf.disgenet.org/resource/gda/DGN00ad8cebfe3b74314e2beccd2e033c45
"gene-disease association linked with genetic variation"@en
"peroxisome proliferator activated receptor alpha [ncbigene:5465] - Hepatitis B [umls:C0019163] Association [disgenet:DGN00ad8cebfe3b74314e2beccd2e033c45]"@en
"Association between the gene [ncbigene:5465] and the disease [umls:C0019163] integrated into DisGeNET. Gene-disease associations are identified by the DisGeNET ID."@en
"peroxisome proliferator activated receptor alpha [ncbigene:5465] - Hepatitis B [umls:C0019163] Association"@en
"disgenet:DGN00ad8cebfe3b74314e2beccd2e033c45"^^<http://www.w3.org/2001/XMLSchema#string>
http://rdf.disgenet.org/v6.0.0/void/geneDiseaseAssociation
http://rdf.disgenet.org/resource/gda/DGN00d03531e47d2238d7b48362cc398608
"gene-disease association linked with genetic variation"@en
"chloride voltage-gated channel 7 [ncbigene:1186] - Osteopetrosis [umls:C0029454] Association [disgenet:DGN00d03531e47d2238d7b48362cc398608]"@en
"Association between the gene [ncbigene:1186] and the disease [umls:C0029454] integrated into DisGeNET. Gene-disease associations are identified by the DisGeNET ID."@en
"chloride voltage-gated channel 7 [ncbigene:1186] - Osteopetrosis [umls:C0029454] Association"@en
"disgenet:DGN00d03531e47d2238d7b48362cc398608"^^<http://www.w3.org/2001/XMLSchema#string>
http://rdf.disgenet.org/v6.0.0/void/geneDiseaseAssociation
http://rdf.disgenet.org/resource/gda/DGN00da4af90a98e4cb879f9c47c15aa98d
"gene-disease association linked with genetic variation"@en
"dynactin subunit 1 [ncbigene:1639] - Motor Neuron Disease [umls:C0085084] Association [disgenet:DGN00da4af90a98e4cb879f9c47c15aa98d]"@en
"Association between the gene [ncbigene:1639] and the disease [umls:C0085084] integrated into DisGeNET. Gene-disease associations are identified by the DisGeNET ID."@en
"dynactin subunit 1 [ncbigene:1639] - Motor Neuron Disease [umls:C0085084] Association"@en
"disgenet:DGN00da4af90a98e4cb879f9c47c15aa98d"^^<http://www.w3.org/2001/XMLSchema#string>
http://rdf.disgenet.org/v6.0.0/void/geneDiseaseAssociation
http://rdf.disgenet.org/resource/gda/DGN00ff4c99f26cc914d20214c2738a073d
"gene-disease association linked with genetic variation"@en
"insulin receptor [ncbigene:3643] - Polycystic Ovary Syndrome [umls:C0032460] Association [disgenet:DGN00ff4c99f26cc914d20214c2738a073d]"@en
"Association between the gene [ncbigene:3643] and the disease [umls:C0032460] integrated into DisGeNET. Gene-disease associations are identified by the DisGeNET ID."@en
"insulin receptor [ncbigene:3643] - Polycystic Ovary Syndrome [umls:C0032460] Association"@en
"disgenet:DGN00ff4c99f26cc914d20214c2738a073d"^^<http://www.w3.org/2001/XMLSchema#string>
http://rdf.disgenet.org/v6.0.0/void/geneDiseaseAssociation
http://rdf.disgenet.org/resource/gda/DGN0111aaa36b14f679be4cc2e29391b59e
"gene-disease association linked with genetic variation"@en
"fibroblast growth factor receptor 2 [ncbigene:2263] - Antley-Bixler Syndrome, Autosomal Dominant [umls:C2936791] Association [disgenet:DGN0111aaa36b14f679be4cc2e29391b59e]"@en
"Association between the gene [ncbigene:2263] and the disease [umls:C2936791] integrated into DisGeNET. Gene-disease associations are identified by the DisGeNET ID."@en
"fibroblast growth factor receptor 2 [ncbigene:2263] - Antley-Bixler Syndrome, Autosomal Dominant [umls:C2936791] Association"@en
"disgenet:DGN0111aaa36b14f679be4cc2e29391b59e"^^<http://www.w3.org/2001/XMLSchema#string>
http://rdf.disgenet.org/v6.0.0/void/geneDiseaseAssociation