<https://rdf.molmedb.upol.cz/reference/ref2271> <http://purl.org/dc/terms/subject> <https://identifiers.org/molmedb/MM474997>,
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	<http://purl.org/ontology/bibo/pmid> "17157021"^^<http://www.w3.org/2001/XMLSchema#string>;
	<http://purl.org/dc/terms/subject> <https://identifiers.org/molmedb/MM496384>,
		<https://identifiers.org/molmedb/MM474992>,
		<https://identifiers.org/molmedb/MM474991>,
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	<http://www.w3.org/1999/02/22-rdf-syntax-ns#type> <http://purl.org/dc/terms/BibliographicResource>;
	<http://purl.org/dc/terms/subject> <https://identifiers.org/molmedb/MM474996>,
		<https://identifiers.org/molmedb/MM474993>,
		<https://identifiers.org/molmedb/MM474995>;
	<http://purl.org/dc/terms/bibliographicCitation> "Barrett DG, Catalano JG, Deaton DN, Long ST, McFadyen RB, Miller AB, Miller LR, Samano V, Tavares FX, Wells-Knecht KJ, Wright LL, Zhou HQ.: Acyclic, orally bioavailable ketone-based cathepsin K inhibitors. Bioorg Med Chem Lett, Volume 17 (1), 2007"^^<http://www.w3.org/2001/XMLSchema#string>;
	<http://purl.org/dc/terms/subject> <https://identifiers.org/molmedb/MM496384.1> .
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<https://rdf.molmedb.upol.cz/interaction/int1008245> <http://www.w3.org/ns/prov#hadPrimarySource> <https://rdf.molmedb.upol.cz/reference/ref2271> .
<https://rdf.molmedb.upol.cz/interaction/int974873> <http://www.w3.org/ns/prov#hadPrimarySource> <https://rdf.molmedb.upol.cz/reference/ref2271> .
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<https://rdf.molmedb.upol.cz/interaction/int974795> <http://www.w3.org/ns/prov#hadPrimarySource> <https://rdf.molmedb.upol.cz/reference/ref2271> .
<https://rdf.molmedb.upol.cz/interaction/int974778> <http://www.w3.org/ns/prov#hadPrimarySource> <https://rdf.molmedb.upol.cz/reference/ref2271> .
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<https://rdf.molmedb.upol.cz/interaction/int974845> <http://www.w3.org/ns/prov#hadPrimarySource> <https://rdf.molmedb.upol.cz/reference/ref2271> .
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<https://rdf.molmedb.upol.cz/interaction/int1008298> <http://www.w3.org/ns/prov#hadPrimarySource> <https://rdf.molmedb.upol.cz/reference/ref2271> .