| Name | neighbor of BRCA1 gene 2 (non-protein coding) |
| Description | This gene was identified by its close proximity on chromosome 17 to tumor suppressor gene BRCA1. Experimental evidence indicates that the two genes share a bi-directional promoter. Transcription for either gene is controlled individually by distinct transcriptional repressor factors. A short (112 amino acid) open reading frame is observed which includes a region derived from a LINE1 element. A strong Kozak signal is not observed for the putative ORF and the stop codon is more than 55 nucleotides upstream of the last splice site for the transcript, suggesting that the transcript is subject to nonsense-mediated decay. Therefore, this gene does not appear to encode a protein. Glucose starvation induces the expression of this gene and the long non-coding RNA transcribed by it functions with AMP-activated protein kinase in mediating the energy stress response. [provided by RefSeq, Aug 2016] |
| Summary |
{"type": "root", "children": [{"type": "p", "children": [{"type": "t", "text": "\nNBR2 is a stress‐induced long non‐coding RNA that is rapidly upregulated under energy deprivation through the LKB1–AMPK pathway. Upon energy stress or pharmacological treatment (e.g., with phenformin), NBR2 directly interacts with AMPK to promote its kinase activity, thereby establishing a feed‐forward loop that reinforces metabolic adaptation. In addition, NBR2 has been shown to modulate glucose uptake—by affecting key transporters such as GLUT1—and to influence autophagic processes in hepatocytes, underscoring its pivotal role in maintaining cellular energy homeostasis and in shaping the metabolic response to stress conditions."}, {"type": "fg", "children": [{"type": "fg_fs", "start_ref": "1", "end_ref": "4"}]}, {"type": "t", "text": "\n"}]}, {"type": "t", "text": "\n\n"}, {"type": "p", "children": [{"type": "t", "text": "\nBeyond its role in metabolic stress adaptation, NBR2 functions as a broad tumor suppressor in various malignancies. In hepatocellular carcinoma, diminished NBR2 expression correlates with enhanced cell proliferation, invasion, migration, and protective autophagy—processes partly mediated via ERK and JNK pathways."}, {"type": "fg", "children": [{"type": "fg_f", "ref": "5"}]}, {"type": "t", "text": " Moreover, studies have explored its modulation by anticancer agents such as curcumin"}, {"type": "fg", "children": [{"type": "fg_f", "ref": "6"}]}, {"type": "t", "text": "and its role in non–small‐cell lung cancer"}, {"type": "fg", "children": [{"type": "fg_f", "ref": "7"}]}, {"type": "t", "text": "as well as lung cancer metabolism."}, {"type": "fg", "children": [{"type": "fg_f", "ref": "8"}]}, {"type": "t", "text": " In colorectal cancer, NBR2 influences the tumor microenvironment by regulating tumor‐associated macrophage polarization toward an antitumoral M1 phenotype through effects on miR‑19a and AMPK/HIF‑1α–AKT/mTOR signaling."}, {"type": "fg", "children": [{"type": "fg_f", "ref": "9"}]}, {"type": "t", "text": " In hepatoblastoma, NBR2 acts as a competing endogenous RNA by binding miR‑22, thereby counteracting miR‑22′s suppression of TCF7 and modulating proliferation, invasion, and apoptosis, particularly under glucose starvation conditions."}, {"type": "fg", "children": [{"type": "fg_f", "ref": "11"}]}, {"type": "t", "text": " Its regulation is further highlighted by a bidirectional promoter shared with BRCA1, where hypoxic conditions lead to increased NBR2 expression despite BRCA1 repression"}, {"type": "fg", "children": [{"type": "fg_f", "ref": "12"}]}, {"type": "t", "text": ", and by its capacity to restrain glioma cell proliferation via p15 downregulation."}, {"type": "fg", "children": [{"type": "fg_f", "ref": "13"}]}, {"type": "t", "text": " Collectively, these findings underscore the multifaceted role of NBR2 in suppressing tumor progression by impinging upon metabolic, autophagic, and microenvironment‐related pathways.\n"}]}, {"type": "rg", "children": [{"type": "r", "ref": 1, "children": [{"type": "t", "text": "Xiaowen Liu, Zhen-Dong Xiao, Leng Han, et al. "}, {"type": "b", "children": [{"type": "t", "text": "LncRNA NBR2 engages a metabolic checkpoint by regulating AMPK under energy stress."}]}, {"type": "t", "text": " "}, {"type": "i", "children": [{"type": "t", "text": "Nat Cell Biol (2016)"}]}, {"type": "t", "text": " DOI: "}, {"type": "a", "children": [{"type": "t", "text": "10.1038/ncb3328"}], "href": "https://doi.org/10.1038/ncb3328"}, {"type": "t", "text": " PMID: "}, {"type": "a", "children": [{"type": "t", "text": "26999735"}], "href": "https://pubmed.ncbi.nlm.nih.gov/26999735"}]}, {"type": "r", "ref": 2, "children": [{"type": "t", "text": "Xiaowen Liu, Boyi Gan "}, {"type": "b", "children": [{"type": "t", "text": "lncRNA NBR2 modulates cancer cell sensitivity to phenformin through GLUT1."}]}, {"type": "t", "text": " "}, {"type": "i", "children": [{"type": "t", "text": "Cell Cycle (2016)"}]}, {"type": "t", "text": " DOI: "}, {"type": "a", "children": [{"type": "t", "text": "10.1080/15384101.2016.1249545"}], "href": "https://doi.org/10.1080/15384101.2016.1249545"}, {"type": "t", "text": " PMID: "}, {"type": "a", "children": [{"type": "t", "text": "27792451"}], "href": "https://pubmed.ncbi.nlm.nih.gov/27792451"}]}, {"type": "r", "ref": 3, "children": [{"type": "t", "text": "Yan-Min Liu, Jin-Hui Ma, Qing-Lei Zeng, et al. "}, {"type": "b", "children": [{"type": "t", "text": "MiR-19a Affects Hepatocyte Autophagy via Regulating lncRNA NBR2 and AMPK/PPARα in D-GalN/Lipopolysaccharide-Stimulated Hepatocytes."}]}, {"type": "t", "text": " "}, {"type": "i", "children": [{"type": "t", "text": "J Cell Biochem (2018)"}]}, {"type": "t", "text": " DOI: "}, {"type": "a", "children": [{"type": "t", "text": "10.1002/jcb.26188"}], "href": "https://doi.org/10.1002/jcb.26188"}, {"type": "t", "text": " PMID: "}, {"type": "a", "children": [{"type": "t", "text": "28586153"}], "href": "https://pubmed.ncbi.nlm.nih.gov/28586153"}]}, {"type": "r", "ref": 4, "children": [{"type": "t", "text": "Chang-Sheng Wang, Xiao-Bo Zhang, Xi-Tian Zhu, et al. "}, {"type": "b", "children": [{"type": "t", "text": "NBR2/miR-561-5p/DLC1 axis inhibited the development of multiple myeloma by activating the AMPK/mTOR pathway to repress glycolysis."}]}, {"type": "t", "text": " "}, {"type": "i", "children": [{"type": "t", "text": "Neoplasma (2022)"}]}, {"type": "t", "text": " DOI: "}, {"type": "a", "children": [{"type": "t", "text": "10.4149/neo_2022_211102N1559"}], "href": "https://doi.org/10.4149/neo_2022_211102N1559"}, {"type": "t", "text": " PMID: "}, {"type": "a", "children": [{"type": "t", "text": "35951458"}], "href": "https://pubmed.ncbi.nlm.nih.gov/35951458"}]}, {"type": "r", "ref": 5, "children": [{"type": "t", "text": "Jia-Qi Sheng, Mu-Ru Wang, Dan Fang, et al. "}, {"type": "b", "children": [{"type": "t", "text": "LncRNA NBR2 inhibits tumorigenesis by regulating autophagy in hepatocellular carcinoma."}]}, {"type": "t", "text": " "}, {"type": "i", "children": [{"type": "t", "text": "Biomed Pharmacother (2021)"}]}, {"type": "t", "text": " DOI: "}, {"type": "a", "children": [{"type": "t", "text": "10.1016/j.biopha.2020.111023"}], "href": "https://doi.org/10.1016/j.biopha.2020.111023"}, {"type": "t", "text": " PMID: "}, {"type": "a", "children": [{"type": "t", "text": "33378941"}], "href": "https://pubmed.ncbi.nlm.nih.gov/33378941"}]}, {"type": "r", "ref": 6, "children": [{"type": "t", "text": "Hua Yu, Yangyang Xie, Zhendong Zhou, et al. "}, {"type": "b", "children": [{"type": "t", "text": "Curcumin Regulates the Progression of Colorectal Cancer via LncRNA NBR2/AMPK Pathway."}]}, {"type": "t", "text": " "}, {"type": "i", "children": [{"type": "t", "text": "Technol Cancer Res Treat (2019)"}]}, {"type": "t", "text": " DOI: "}, {"type": "a", "children": [{"type": "t", "text": "10.1177/1533033819870781"}], "href": "https://doi.org/10.1177/1533033819870781"}, {"type": "t", "text": " PMID: "}, {"type": "a", "children": [{"type": "t", "text": "31888414"}], "href": "https://pubmed.ncbi.nlm.nih.gov/31888414"}]}, {"type": "r", "ref": 7, "children": [{"type": "t", "text": "Y-P Gao, Y Li, H-J Li, et al. "}, {"type": "b", "children": [{"type": "t", "text": "LncRNA NBR2 inhibits EMT progression by regulating Notch1 pathway in NSCLC."}]}, {"type": "t", "text": " "}, {"type": "i", "children": [{"type": "t", "text": "Eur Rev Med Pharmacol Sci (2019)"}]}, {"type": "t", "text": " DOI: "}, {"type": "a", "children": [{"type": "t", "text": "10.26355/eurrev_201909_19011"}], "href": "https://doi.org/10.26355/eurrev_201909_19011"}, {"type": "t", "text": " PMID: "}, {"type": "a", "children": [{"type": "t", "text": "31599420"}], "href": "https://pubmed.ncbi.nlm.nih.gov/31599420"}]}, {"type": "r", "ref": 8, "children": [{"type": "t", "text": "Jun Huang, Qiuhua Yu, Junjie Zhang, et al. "}, {"type": "b", "children": [{"type": "t", "text": "LncRNA NBR2 Regulates Cancer Cell Stemness and Predicts Survival in Non-small Cell Cancer Patients by Downregulating TGF-β1."}]}, {"type": "t", "text": " "}, {"type": "i", "children": [{"type": "t", "text": "Curr Pharm Biotechnol (2023)"}]}, {"type": "t", "text": " DOI: "}, {"type": "a", "children": [{"type": "t", "text": "10.2174/1389201023666220728143410"}], "href": "https://doi.org/10.2174/1389201023666220728143410"}, {"type": "t", "text": " PMID: "}, {"type": "a", "children": [{"type": "t", "text": "35909269"}], "href": "https://pubmed.ncbi.nlm.nih.gov/35909269"}]}, {"type": "r", "ref": 9, "children": [{"type": "t", "text": "Fuji Lai, Huiqin Zhang, Binbin Xu, et al. "}, {"type": "b", "children": [{"type": "t", "text": "Long non-coding RNA NBR2 suppresses the progress of colorectal cancer in vitro and in vivo by regulating the polarization of TAM."}]}, {"type": "t", "text": " "}, {"type": "i", "children": [{"type": "t", "text": "Bioengineered (2021)"}]}, {"type": "t", "text": " DOI: "}, {"type": "a", "children": [{"type": "t", "text": "10.1080/21655979.2021.1958558"}], "href": "https://doi.org/10.1080/21655979.2021.1958558"}, {"type": "t", "text": " PMID: "}, {"type": "a", "children": [{"type": "t", "text": "34506209"}], "href": "https://pubmed.ncbi.nlm.nih.gov/34506209"}]}, {"type": "r", "ref": 10, "children": [{"type": "t", "text": "Xiaoting Yang, Ye Luo, Mengying Li, et al. "}, {"type": "b", "children": [{"type": "t", "text": "Long non-coding RNA NBR2 suppresses the progression of colorectal cancer by downregulating miR-19a to regulate M2 macrophage polarization."}]}, {"type": "t", "text": " "}, {"type": "i", "children": [{"type": "t", "text": "Chin J Physiol (2023)"}]}, {"type": "t", "text": " DOI: "}, {"type": "a", "children": [{"type": "t", "text": "10.4103/cjop.CJOP-D-23-00064"}], "href": "https://doi.org/10.4103/cjop.CJOP-D-23-00064"}, {"type": "t", "text": " PMID: "}, {"type": "a", "children": [{"type": "t", "text": "38149567"}], "href": "https://pubmed.ncbi.nlm.nih.gov/38149567"}]}, {"type": "r", "ref": 11, "children": [{"type": "t", "text": "Chengguang Zhu, Xiangling He, Keke Chen, et al. "}, {"type": "b", "children": [{"type": "t", "text": "LncRNA NBR2 aggravates hepatoblastoma cell malignancy and promotes cell proliferation under glucose starvation through the miR-22/TCF7 axis."}]}, {"type": "t", "text": " "}, {"type": "i", "children": [{"type": "t", "text": "Cell Cycle (2021)"}]}, {"type": "t", "text": " DOI: "}, {"type": "a", "children": [{"type": "t", "text": "10.1080/15384101.2021.1885236"}], "href": "https://doi.org/10.1080/15384101.2021.1885236"}, {"type": "t", "text": " PMID: "}, {"type": "a", "children": [{"type": "t", "text": "33651649"}], "href": "https://pubmed.ncbi.nlm.nih.gov/33651649"}]}, {"type": "r", "ref": 12, "children": [{"type": "t", "text": "J Erin Wiedmeier, Anna Ohlrich, Adrian Chu, et al. "}, {"type": "b", "children": [{"type": "t", "text": "Induction of the long noncoding RNA NBR2 from the bidirectional BRCA1 promoter under hypoxic conditions."}]}, {"type": "t", "text": " "}, {"type": "i", "children": [{"type": "t", "text": "Mutat Res (2017)"}]}, {"type": "t", "text": " DOI: "}, {"type": "a", "children": [{"type": "t", "text": "10.1016/j.mrfmmm.2017.02.001"}], "href": "https://doi.org/10.1016/j.mrfmmm.2017.02.001"}, {"type": "t", "text": " PMID: "}, {"type": "a", "children": [{"type": "t", "text": "28249151"}], "href": "https://pubmed.ncbi.nlm.nih.gov/28249151"}]}, {"type": "r", "ref": 13, "children": [{"type": "t", "text": "Jianjun Zhang, Hongsheng Jiang, Xuequan Feng, et al. "}, {"type": "b", "children": [{"type": "t", "text": "NBR2 promotes the proliferation of glioma cells via inhibiting p15 expression."}]}, {"type": "t", "text": " "}, {"type": "i", "children": [{"type": "t", "text": "J BUON (2021)"}]}, {"type": "t", "text": " PMID: "}, {"type": "a", "children": [{"type": "t", "text": "34076984"}], "href": "https://pubmed.ncbi.nlm.nih.gov/34076984"}]}]}]}
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| Synonyms | NCRNA00192 |
| Proteins | NBR2_HUMAN |
| NCBI Gene ID | 10230 |
| API | |
| Download Associations | |
| Predicted Functions |
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| Co-expressed Genes |
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| Expression in Tissues and Cell Lines |
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NBR2 has 3,469 functional associations with biological entities spanning 8 categories (molecular profile, organism, chemical, functional term, phrase or reference, disease, phenotype or trait, cell line, cell type or tissue, gene, protein or microRNA, sequence feature) extracted from 45 datasets.
Click the + buttons to view associations for NBR2 from the datasets below.
If available, associations are ranked by standardized value
| Dataset | Summary | |
|---|---|---|
| Allen Brain Atlas Adult Human Brain Tissue Gene Expression Profiles | tissues with high or low expression of NBR2 gene relative to other tissues from the Allen Brain Atlas Adult Human Brain Tissue Gene Expression Profiles dataset. | |
| Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray | tissue samples with high or low expression of NBR2 gene relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray dataset. | |
| Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq | tissue samples with high or low expression of NBR2 gene relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq dataset. | |
| Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles | tissues with high or low expression of NBR2 gene relative to other tissues from the Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles dataset. | |
| BioGPS Cell Line Gene Expression Profiles | cell lines with high or low expression of NBR2 gene relative to other cell lines from the BioGPS Cell Line Gene Expression Profiles dataset. | |
| BioGPS Human Cell Type and Tissue Gene Expression Profiles | cell types and tissues with high or low expression of NBR2 gene relative to other cell types and tissues from the BioGPS Human Cell Type and Tissue Gene Expression Profiles dataset. | |
| CCLE Cell Line Gene CNV Profiles | cell lines with high or low copy number of NBR2 gene relative to other cell lines from the CCLE Cell Line Gene CNV Profiles dataset. | |
| CCLE Cell Line Gene Expression Profiles | cell lines with high or low expression of NBR2 gene relative to other cell lines from the CCLE Cell Line Gene Expression Profiles dataset. | |
| ChEA Transcription Factor Binding Site Profiles | transcription factor binding site profiles with transcription factor binding evidence at the promoter of NBR2 gene from the CHEA Transcription Factor Binding Site Profiles dataset. | |
| ChEA Transcription Factor Targets | transcription factors binding the promoter of NBR2 gene in low- or high-throughput transcription factor functional studies from the CHEA Transcription Factor Targets dataset. | |
| CMAP Signatures of Differentially Expressed Genes for Small Molecules | small molecule perturbations changing expression of NBR2 gene from the CMAP Signatures of Differentially Expressed Genes for Small Molecules dataset. | |
| COMPARTMENTS Text-mining Protein Localization Evidence Scores | cellular components co-occuring with NBR2 protein in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores dataset. | |
| COSMIC Cell Line Gene CNV Profiles | cell lines with high or low copy number of NBR2 gene relative to other cell lines from the COSMIC Cell Line Gene CNV Profiles dataset. | |
| COSMIC Cell Line Gene Mutation Profiles | cell lines with NBR2 gene mutations from the COSMIC Cell Line Gene Mutation Profiles dataset. | |
| DISEASES Text-mining Gene-Disease Association Evidence Scores | diseases co-occuring with NBR2 gene in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset. | |
| ENCODE Histone Modification Site Profiles | histone modification site profiles with high histone modification abundance at NBR2 gene from the ENCODE Histone Modification Site Profiles dataset. | |
| ENCODE Transcription Factor Binding Site Profiles | transcription factor binding site profiles with transcription factor binding evidence at the promoter of NBR2 gene from the ENCODE Transcription Factor Binding Site Profiles dataset. | |
| ENCODE Transcription Factor Targets | transcription factors binding the promoter of NBR2 gene in ChIP-seq datasets from the ENCODE Transcription Factor Targets dataset. | |
| GDSC Cell Line Gene Expression Profiles | cell lines with high or low expression of NBR2 gene relative to other cell lines from the GDSC Cell Line Gene Expression Profiles dataset. | |
| GeneSigDB Published Gene Signatures | PubMedIDs of publications reporting gene signatures containing NBR2 from the GeneSigDB Published Gene Signatures dataset. | |
| GEO Signatures of Differentially Expressed Genes for Gene Perturbations | gene perturbations changing expression of NBR2 gene from the GEO Signatures of Differentially Expressed Genes for Gene Perturbations dataset. | |
| GEO Signatures of Differentially Expressed Genes for Kinase Perturbations | kinase perturbations changing expression of NBR2 gene from the GEO Signatures of Differentially Expressed Genes for Kinase Perturbations dataset. | |
| GEO Signatures of Differentially Expressed Genes for Small Molecules | small molecule perturbations changing expression of NBR2 gene from the GEO Signatures of Differentially Expressed Genes for Small Molecules dataset. | |
| GEO Signatures of Differentially Expressed Genes for Transcription Factor Perturbations | transcription factor perturbations changing expression of NBR2 gene from the GEO Signatures of Differentially Expressed Genes for Transcription Factor Perturbations dataset. | |
| GEO Signatures of Differentially Expressed Genes for Viral Infections | virus perturbations changing expression of NBR2 gene from the GEO Signatures of Differentially Expressed Genes for Viral Infections dataset. | |
| GTEx eQTL | SNPs regulating expression of NBR2 gene from the GTEx eQTL dataset. | |
| GTEx Tissue Gene Expression Profiles | tissues with high or low expression of NBR2 gene relative to other tissues from the GTEx Tissue Gene Expression Profiles dataset. | |
| GTEx Tissue Sample Gene Expression Profiles | tissue samples with high or low expression of NBR2 gene relative to other tissue samples from the GTEx Tissue Sample Gene Expression Profiles dataset. | |
| GTEx Tissue-Specific Aging Signatures | tissue samples with high or low expression of NBR2 gene relative to other tissue samples from the GTEx Tissue-Specific Aging Signatures dataset. | |
| GWASdb SNP-Disease Associations | diseases associated with NBR2 gene in GWAS and other genetic association datasets from the GWASdb SNP-Disease Associations dataset. | |
| GWASdb SNP-Phenotype Associations | phenotypes associated with NBR2 gene in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. | |
| Heiser et al., PNAS, 2011 Cell Line Gene Expression Profiles | cell lines with high or low expression of NBR2 gene relative to other cell lines from the Heiser et al., PNAS, 2011 Cell Line Gene Expression Profiles dataset. | |
| JASPAR Predicted Transcription Factor Targets | transcription factors regulating expression of NBR2 gene predicted using known transcription factor binding site motifs from the JASPAR Predicted Transcription Factor Targets dataset. | |
| Klijn et al., Nat. Biotechnol., 2015 Cell Line Gene CNV Profiles | cell lines with high or low copy number of NBR2 gene relative to other cell lines from the Klijn et al., Nat. Biotechnol., 2015 Cell Line Gene CNV Profiles dataset. | |
| Klijn et al., Nat. Biotechnol., 2015 Cell Line Gene Expression Profiles | cell lines with high or low expression of NBR2 gene relative to other cell lines from the Klijn et al., Nat. Biotechnol., 2015 Cell Line Gene Expression Profiles dataset. | |
| KnockTF Gene Expression Profiles with Transcription Factor Perturbations | transcription factor perturbations changing expression of NBR2 gene from the KnockTF Gene Expression Profiles with Transcription Factor Perturbations dataset. | |
| LINCS L1000 CMAP Chemical Perturbation Consensus Signatures | small molecule perturbations changing expression of NBR2 gene from the LINCS L1000 CMAP Chemical Perturbations Consensus Signatures dataset. | |
| LOCATE Predicted Protein Localization Annotations | cellular components predicted to contain NBR2 protein from the LOCATE Predicted Protein Localization Annotations dataset. | |
| MotifMap Predicted Transcription Factor Targets | transcription factors regulating expression of NBR2 gene predicted using known transcription factor binding site motifs from the MotifMap Predicted Transcription Factor Targets dataset. | |
| Roadmap Epigenomics Cell and Tissue DNA Methylation Profiles | cell types and tissues with high or low DNA methylation of NBR2 gene relative to other cell types and tissues from the Roadmap Epigenomics Cell and Tissue DNA Methylation Profiles dataset. | |
| Roadmap Epigenomics Cell and Tissue Gene Expression Profiles | cell types and tissues with high or low expression of NBR2 gene relative to other cell types and tissues from the Roadmap Epigenomics Cell and Tissue Gene Expression Profiles dataset. | |
| Roadmap Epigenomics Histone Modification Site Profiles | histone modification site profiles with high histone modification abundance at NBR2 gene from the Roadmap Epigenomics Histone Modification Site Profiles dataset. | |
| TCGA Signatures of Differentially Expressed Genes for Tumors | tissue samples with high or low expression of NBR2 gene relative to other tissue samples from the TCGA Signatures of Differentially Expressed Genes for Tumors dataset. | |
| TISSUES Experimental Tissue Protein Expression Evidence Scores | tissues with high expression of NBR2 protein in proteomics datasets from the TISSUES Experimental Tissue Protein Expression Evidence Scores dataset. | |
| TISSUES Text-mining Tissue Protein Expression Evidence Scores | tissues co-occuring with NBR2 protein in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores dataset. | |
