The API interface can be invoked by users using a broad range of programming languages (python, Java, etc.), and all association data can be retrieved by providing the association identifier (ass_id) in ncRPheno, such as ncRP########.
| Example url: http://lilab2.sysu.edu.cn/ncrpheno/ncrphedb/association?ass_id=ncRP00150000 |
|---|
Optional parameter: Association identifier(ass_id) (12 characters)---This is the association identifier in ncRPheno, e.g. ncRP00150000.
{"Results":[{"ncRPheDB_ID":"ncRP00150000","ncRNA_Symbol":"TUNAR","associations":[{"ncRPheDB_ID":"ncRP00150000","ncRNA_Symbol":"TUNAR","disease_Name":null,"methods":"qRT-PCR","pmid":"24530304","disease_Name_1":"Huntington's disease","expression_pattern_or_Mutation":"Association","eco":"ECO:0005516: molecule detection assay evidence","sample_Name":"brain","treatment":"N/A","datasources":"LncRNADiseaseV2","title":"An evolutionarily conserved long noncoding RNA TUNA controls pluripotency and neural lineage commitment.","description":"TUNA expression in the brains of Huntington¡¯s patients was significantly associated with disease grade.","target":"N/A"}],"ncRNAs":[{"ncRNA_Symbol":"TUNAR","ncRNA_ID":"URS00008E3A31","snps":"N/A","targets":"N/A","ensembl":"N/A","category":"lncRNA","species":"Homo sapiens"}],"disease":{"disease_Name":"Huntington disease","ontology_ID":"Orphanet_399","alternativeName":"Huntington chorea","definition":"Huntington disease (HD) is a rare neurodegenerative disorder of the central nervous system characterized by unwanted choreatic movements, behavioral and psychiatric disturbances and dementia."},"score":"0.181","disease_Name":"Huntington disease","ontology_ID":"Orphanet_399","category":"lncRNA","species":"Homo sapiens","node":"Neurodegenerative disease with chorea"}]}