Toward better drug discovery with knowledge graph

2022 ◽  
Vol 72 ◽  
pp. 114-126
Author(s):  
Xiangxiang Zeng ◽  
Xinqi Tu ◽  
Yuansheng Liu ◽  
Xiangzheng Fu ◽  
Yansen Su
Genes ◽  
2021 ◽  
Vol 12 (7) ◽  
pp. 998
Author(s):  
Peng Zhang ◽  
Yi Bu ◽  
Peng Jiang ◽  
Xiaowen Shi ◽  
Bing Lun ◽  
...  

This study builds a coronavirus knowledge graph (KG) by merging two information sources. The first source is Analytical Graph (AG), which integrates more than 20 different public datasets related to drug discovery. The second source is CORD-19, a collection of published scientific articles related to COVID-19. We combined both chemo genomic entities in AG with entities extracted from CORD-19 to expand knowledge in the COVID-19 domain. Before populating KG with those entities, we perform entity disambiguation on CORD-19 collections using Wikidata. Our newly built KG contains at least 21,700 genes, 2500 diseases, 94,000 phenotypes, and other biological entities (e.g., compound, species, and cell lines). We define 27 relationship types and use them to label each edge in our KG. This research presents two cases to evaluate the KG’s usability: analyzing a subgraph (ego-centered network) from the angiotensin-converting enzyme (ACE) and revealing paths between biological entities (hydroxychloroquine and IL-6 receptor; chloroquine and STAT1). The ego-centered network captured information related to COVID-19. We also found significant COVID-19-related information in top-ranked paths with a depth of three based on our path evaluation.


2018 ◽  
Vol 19 (1) ◽  
Author(s):  
Shengtian Sang ◽  
Zhihao Yang ◽  
Lei Wang ◽  
Xiaoxia Liu ◽  
Hongfei Lin ◽  
...  

Author(s):  
Kara Schatz ◽  
Cleber Melo-Filho ◽  
Alexander Tropsha ◽  
Rada Chirkova

Pharmaceutics ◽  
2021 ◽  
Vol 13 (6) ◽  
pp. 794
Author(s):  
Kevin McCoy ◽  
Sateesh Gudapati ◽  
Lawrence He ◽  
Elaina Horlander ◽  
David Kartchner ◽  
...  

Link prediction in artificial intelligence is used to identify missing links or derive future relationships that can occur in complex networks. A link prediction model was developed using the complex heterogeneous biomedical knowledge graph, SemNet, to predict missing links in biomedical literature for drug discovery. A web application visualized knowledge graph embeddings and link prediction results using TransE, CompleX, and RotatE based methods. The link prediction model achieved up to 0.44 hits@10 on the entity prediction tasks. The recent outbreak of severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2), also known as COVID-19, served as a case study to demonstrate the efficacy of link prediction modeling for drug discovery. The link prediction algorithm guided identification and ranking of repurposed drug candidates for SARS-CoV-2 primarily by text mining biomedical literature from previous coronaviruses, including SARS and middle east respiratory syndrome (MERS). Repurposed drugs included potential primary SARS-CoV-2 treatment, adjunctive therapies, or therapeutics to treat side effects. The link prediction accuracy for nodes ranked highly for SARS coronavirus was 0.875 as calculated by human in the loop validation on existing COVID-19 specific data sets. Drug classes predicted as highly ranked include anti-inflammatory, nucleoside analogs, protease inhibitors, antimalarials, envelope proteins, and glycoproteins. Examples of highly ranked predicted links to SARS-CoV-2: human leukocyte interferon, recombinant interferon-gamma, cyclosporine, antiviral therapy, zidovudine, chloroquine, vaccination, methotrexate, artemisinin, alkaloids, glycyrrhizic acid, quinine, flavonoids, amprenavir, suramin, complement system proteins, fluoroquinolones, bone marrow transplantation, albuterol, ciprofloxacin, quinolone antibacterial agents, and hydroxymethylglutaryl-CoA reductase inhibitors. Approximately 40% of identified drugs were not previously connected to SARS, such as edetic acid or biotin. In summary, link prediction can effectively suggest repurposed drugs for emergent diseases.


IEEE Access ◽  
2019 ◽  
Vol 7 ◽  
pp. 8404-8415 ◽  
Author(s):  
Shengtian Sang ◽  
Zhihao Yang ◽  
Xiaoxia Liu ◽  
Lei Wang ◽  
Hongfei Lin ◽  
...  

Author(s):  
Masaki Asada ◽  
Nallappan Gunasekaran ◽  
Makoto Miwa ◽  
Yutaka Sasaki

We deal with a heterogeneous pharmaceutical knowledge-graph containing textual information built from several databases. The knowledge graph is a heterogeneous graph that includes a wide variety of concepts and attributes, some of which are provided in the form of textual pieces of information which have not been targeted in the conventional graph completion tasks. To investigate the utility of textual information for knowledge graph completion, we generate embeddings from textual descriptions given to heterogeneous items, such as drugs and proteins, while learning knowledge graph embeddings. We evaluate the obtained graph embeddings on the link prediction task for knowledge graph completion, which can be used for drug discovery and repurposing. We also compare the results with existing methods and discuss the utility of the textual information.


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