@prefix dcterms: . @prefix np: . @prefix npx: . @prefix ns1: . @prefix ns2: . @prefix ntemplate: . @prefix orcid: . @prefix owl: . @prefix prov: . @prefix rdfs: . @prefix skos: . @prefix sub: . @prefix this: . @prefix xsd: . sub:Head { this: a np:Nanopublication; np:hasAssertion sub:assertion; np:hasProvenance sub:provenance; np:hasPublicationInfo sub:pubinfo . } sub:assertion { sub:_b1 a ns1:ContextAlias; ns2:alternateName "aaval"; ns2:identifier "short_name"; ns1:hasContext . a owl:Class; dcterms:isPartOf ; ns2:alternateName "AAVal", "AAVal"@nl-be; ns2:comment "comments: Should parent compound not be acrylamide? INCHIKEY Does not seem to correspond to the correct compound Pubchem link to AAVal: https://pubchem.ncbi.nlm.nih.gov/substance/341427830 vs Pubchem link to related compound with INCHI key specified here: https://pubchem.ncbi.nlm.nih.gov/compound/N-_3-Amino-3-oxopropyl_-L-valine --> chemical structure is not the same so I don't know if these are the same compounds? feedback_epi team: Yes assigning Acrylamide as parent compound seems correct to me. Because Acrylamide is the substance a human is exposed to, and we can measure GAVAL and AAVAL to reflect that exposure. GA‑Val (GAVAL) and AA‑Val (AAVAL) — are both well‑established biomarkers of exposure to acrylamide and its metabolite glycidamide. These adducts form when the reactive compounds bind to the N‑terminal valine of hemoglobin. Core attribution - AAVAL (N‑(2‑carbamoylethyl)valine) reflects exposure to acrylamide, the parent compound. - GAVAL (N‑(2‑carbamoyl‑2‑hydroxyethyl)valine) reflects exposure to glycidamide, which is the epoxide metabolite formed when acrylamide is metabolized via CYP2E1. This relationship is well documented: acrylamide is converted to glycidamide, and both acrylamide and glycidamide form hemoglobin adducts that can be used to reconstruct exposure. source: https://pmc.ncbi.nlm.nih.gov/articles/PMC5696489/ Moreover, AA and GA react with plasma and other proteins, such as hemoglobin (Hb). Covalent binding to the N-terminal valine (Val) residue of Hb results in formation of N-(2-carbamoylethyl)valine (AAVal) and N-(2-carbamoyl-2-hydroxyethyl)valine (GAVal) Hb adducts that can be specifically cleaved off and derivatized to serve as biomarkers for long-term exposure monitoring (Bergmark et al. 1993; EFSA 2015; Fennell et al. 2005)."; rdfs:label "N-(2-Carbamoylethyl)valine", "N-(2-Carbamoylethyl)valine"@nl-be; rdfs:subClassOf ns1:BioChemEntity; skos:exactMatch ; ns1:hasContextAlias sub:_b1; ns1:hasGroupLabel "acrylamide"; ns1:isMetaboliteOf . } sub:provenance { sub:assertion prov:generatedAtTime "2026-06-30T20:44:32.879453+02:00"^^xsd:dateTime; prov:wasAttributedTo orcid:0000-0001-8327-0142 . } sub:pubinfo { this: dcterms:license ; npx:hasNanopubType ns1:BioChemEntity; npx:introduces ; rdfs:label "N-(2-Carbamoylethyl)valine"; prov:generatedAtTime "2026-06-30T20:44:32.879453+02:00"^^xsd:dateTime; prov:wasAttributedTo orcid:0000-0002-1825-0097; ntemplate:wasCreatedFromTemplate . sub:sig npx:hasAlgorithm "RSA"; npx:hasPublicKey "MIGfMA0GCSqGSIb3DQEBAQUAA4GNADCBiQKBgQD3RHyHR7WWKBYevw1qK86B6RVzI7oKlvghqXvbpOAX1KueDE6Itru34HRhrVy4OMLCRQWBE3VXktKdbgOxD3vC4cIxz5LX+XOgGWzv5WKSjOfXu/yIeJrzsuIkyHvw7/tToGrE0itJ1wGylJv+YieizmGvNiUHhP0J0+YFMNnvewIDAQAB"; npx:hasSignature "eojsQhr/esDw1B1hMCaI81mGj+lgXvpVXfKbn2Z5HYlaMketa3rJ8vgmXik/5qRE0EpNvUG9hc34k+j9P1ekJC+0bKhiFRNLtcGFcDv7AHn3dyYDZnmKxbRnbFpVy91+BGWgvBOyKSWVrjwYlhOfDja+pPaUTVmhXnVQWSn5aPc="; npx:hasSignatureTarget this:; npx:signedBy orcid:0000-0002-1825-0097 . }