@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 .
}