@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 "2026-06-30T21:05:50.681522+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 "2026-06-30T21:05:50.681522+02:00"^^xsd:dateTime; prov:wasAttributedTo ; ntemplate:wasCreatedFromTemplate . sub:sig npx:hasAlgorithm "RSA"; npx:hasPublicKey "MIIBIjANBgkqhkiG9w0BAQEFAAOCAQ8AMIIBCgKCAQEArwKYgWZTyvZqlmCnnhp2LFM62fX6ZMq4EJ92Oea5H7vHoPOftYej+zS3Vi95eMLZ+RCGd0mNZ0x2+n2rYdGqf/R+9VesqVAjrhGECXLwF3t84VbysGYgiOd5m4YPpzzcgRHpBjYjK86+hR7hqc+y0ai36tYp165WhuaXbnWY5apw8aUN9Q5e1Daid70PST0Hri9dV/Eq4mxbogXlzJbgduIVOwQMyYlGLrb+NyLDpFT+8VpPs+vblnFTF0xwIrcA11O0Mv/WqCfyrtA77nxtc4gY9RkES+2vaEUuCzxbDleUL/JmxOxSI8Cl0LtgBcRZpD7wppe4sIp3CsuK4a5J2QIDAQAB"; npx:hasSignature "gUVwnG2j26ZzBr/bRg2s/E6lLg6thHItHuVDDSaFKMyYZwSPHTk7EqhlsJghtgJnqRZPJsYWs58ZOnVe4nx7+AlDavCYm0r/feFP3WLKCF90UE0CeeRbBitVPtO3xgNokeqj+GyHOCJms7MT2+jzs6U9V0cmu1rZ5+xMrmFQYrEE6glYHDMNnova2aY37taW4zhw5/7ikBoKBIkX0ZvBQxbyP7AjxWaOOvOEhwL7Agt2T0Z6kRYwLyrpC2Vs2JL5NaWcq1b1ENWr3+E0UtR4/M8rGhkiU/rL2kF7WIKWagX8X5Sq8d65ipTvO923ISoACoxVajcOL8puySnSa5H6Aw=="; npx:hasSignatureTarget this:; npx:signedBy . }