http://rdf.ncbi.nlm.nih.gov/pubchem/reference/12001888

Outgoing Links

Predicate Object
contentType Journal Article|Research Support, N.I.H., Extramural|Research Support, Non-U.S. Gov't
endingPage 4531
issn 1520-5126
0002-7863
issueIdentifier 13
pageRange 4530-4531
publicationName Journal of the American Chemical Society
startingPage 4530
hasFundingAgency http://rdf.ncbi.nlm.nih.gov/pubchem/organization/MD5_a1ebfe17b0713ecaf89801f0370c078d
isSupportedBy http://rdf.ncbi.nlm.nih.gov/pubchem/grant/MD5_703284f65031093e95c62fa649ba038c
http://rdf.ncbi.nlm.nih.gov/pubchem/grant/MD5_555c88bcc4af347c88b3580b849b3faa
http://rdf.ncbi.nlm.nih.gov/pubchem/grant/MD5_a4957cd6e367ed56e616641de45d1584
bibliographicCitation Zhou H, Qiao K, Gao Z, Meehan MJ, Li JW, Zhao X, Dorrestein PC, Vederas JC, Tang Y. Enzymatic synthesis of resorcylic acid lactones by cooperation of fungal iterative polyketide synthases involved in hypothemycin biosynthesis. J Am Chem Soc. 2010 Apr 07;132(13):4530–1. PMID: 20222707; PMCID: PMC2861853.
creator http://rdf.ncbi.nlm.nih.gov/pubchem/author/MD5_d12453f24854fc8158da0a616f21e34f
http://rdf.ncbi.nlm.nih.gov/pubchem/author/MD5_3e349e59d5d2167fc88d71713c98f6f4
http://rdf.ncbi.nlm.nih.gov/pubchem/author/MD5_159a444be69779255f154229bb548672
http://rdf.ncbi.nlm.nih.gov/pubchem/author/MD5_3f2afcd87d851654c8ef509aa8b2c4e1
http://rdf.ncbi.nlm.nih.gov/pubchem/author/MD5_ea3fabfb5656bed08b0ee62a61fe1db4
http://rdf.ncbi.nlm.nih.gov/pubchem/author/MD5_0489c9ee1b85380e77f1438776c84721
http://rdf.ncbi.nlm.nih.gov/pubchem/author/ORCID_0000-0002-8176-0727
http://rdf.ncbi.nlm.nih.gov/pubchem/author/MD5_69593aa75855cfa91d19af0bc2f1829f
http://rdf.ncbi.nlm.nih.gov/pubchem/author/MD5_67201f60437edf4ab4d5cd120f42585a
http://rdf.ncbi.nlm.nih.gov/pubchem/author/MD5_d8840f2696964cbab37271c491a777ab
date 2010-03-11-04:00^^<http://www.w3.org/2001/XMLSchema#date>
identifier https://pubmed.ncbi.nlm.nih.gov/PMC2861853
https://doi.org/10.1021/ja100060k
https://pubmed.ncbi.nlm.nih.gov/20222707
isPartOf https://portal.issn.org/resource/ISSN/0002-7863
http://rdf.ncbi.nlm.nih.gov/pubchem/journal/4435
https://portal.issn.org/resource/ISSN/1520-5126
language English
source https://pubmed.ncbi.nlm.nih.gov/
https://www.crossref.org/
title Enzymatic Synthesis of Resorcylic Acid Lactones by Cooperation of Fungal Iterative Polyketide Synthases Involved in Hypothemycin Biosynthesis
discusses http://id.nlm.nih.gov/mesh/M0171396
http://id.nlm.nih.gov/mesh/M0023120
http://id.nlm.nih.gov/mesh/M0012175
http://id.nlm.nih.gov/mesh/M0332882
hasPrimarySubjectTerm http://id.nlm.nih.gov/mesh/D048630Q000378
http://id.nlm.nih.gov/mesh/D007783Q000378
http://id.nlm.nih.gov/mesh/D006999Q000201
http://id.nlm.nih.gov/mesh/D007783Q000737
hasSubjectTerm http://id.nlm.nih.gov/mesh/D015025Q000096
http://id.nlm.nih.gov/mesh/D015025Q000737
http://id.nlm.nih.gov/mesh/D015025Q000031
http://id.nlm.nih.gov/mesh/D015394
discussesAsDerivedByTextMining http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID644066
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID71312102
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID10249057
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID15983949
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID68154
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID5462310
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID5884
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID9929643
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID52945042
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID10270986
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID73075931
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID53315137
http://rdf.ncbi.nlm.nih.gov/pubchem/gene/MD5_b77e41c8d2fcc93d222a4b7c254e1d72
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID131676399
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID129671288
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID19

Incoming Links

Predicate Subject
isDiscussedBy http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID129937238
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID136210299
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID135941462

Total number of triples: 65.