<https://rdf.molmedb.upol.cz/reference/ref1011> <http://purl.org/dc/terms/subject> <https://identifiers.org/molmedb/MM00085>,
		<https://rdf.molmedb.upol.cz/interaction/method33>,
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		<https://identifiers.org/molmedb/MM00768>;
	<http://www.w3.org/1999/02/22-rdf-syntax-ns#type> <http://purl.org/dc/terms/BibliographicResource>;
	<http://purl.org/ontology/bibo/doi> "10.1007/s00044-004-0021-y"^^<http://www.w3.org/2001/XMLSchema#string>;
	<http://purl.org/dc/terms/subject> <https://rdf.molmedb.upol.cz/interaction/membrane21>,
		<https://identifiers.org/molmedb/MM00735>;
	<http://purl.org/dc/terms/bibliographicCitation> "Rawson, D., Dack, K., Dickinson, R. et al. The Design and Synthesis of a Novel, Orally Active, Selective ETA Antagonist. Med Chem Res 13, 149–157 (2004). https://doi.org/10.1007/s00044-004-0021-y"^^<http://www.w3.org/2001/XMLSchema#string> .
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<https://rdf.molmedb.upol.cz/interaction/int18133> <http://www.w3.org/ns/prov#hadPrimarySource> <https://rdf.molmedb.upol.cz/reference/ref1011> .
<https://rdf.molmedb.upol.cz/interaction/int18137> <http://www.w3.org/ns/prov#hadPrimarySource> <https://rdf.molmedb.upol.cz/reference/ref1011> .
<https://rdf.molmedb.upol.cz/interaction/int18132> <http://www.w3.org/ns/prov#hadPrimarySource> <https://rdf.molmedb.upol.cz/reference/ref1011> .
<https://rdf.molmedb.upol.cz/interaction/int18136> <http://www.w3.org/ns/prov#hadPrimarySource> <https://rdf.molmedb.upol.cz/reference/ref1011> .
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<https://rdf.molmedb.upol.cz/interaction/int18135> <http://www.w3.org/ns/prov#hadPrimarySource> <https://rdf.molmedb.upol.cz/reference/ref1011> .
<https://rdf.molmedb.upol.cz/interaction/int18138> <http://www.w3.org/ns/prov#hadPrimarySource> <https://rdf.molmedb.upol.cz/reference/ref1011> .
<https://rdf.molmedb.upol.cz/interaction/int18139> <http://www.w3.org/ns/prov#hadPrimarySource> <https://rdf.molmedb.upol.cz/reference/ref1011> .
